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In-depth proteomic analyses of Haliotis laevigata (greenlip abalone) nacre and prismatic organic shell matrix
Proteome Science volume 16, Article number: 11 (2018)
The shells of various Haliotis species have served as models of invertebrate biomineralization and physical shell properties for more than 20 years. A focus of this research has been the nacreous inner layer of the shell with its conspicuous arrangement of aragonite platelets, resembling in cross-section a brick-and-mortar wall. In comparison, the outer, less stable, calcitic prismatic layer has received much less attention. One of the first molluscan shell proteins to be characterized at the molecular level was Lustrin A, a component of the nacreous organic matrix of Haliotis rufescens. This was soon followed by the C-type lectin perlucin and the growth factor-binding perlustrin, both isolated from H. laevigata nacre, and the crystal growth-modulating AP7 and AP24, isolated from H. rufescens nacre. Mass spectrometry-based proteomics was subsequently applied to to Haliotis biomineralization research with the analysis of the H. asinina shell matrix and yielded 14 different shell-associated proteins. That study was the most comprehensive for a Haliotis species to date.
The shell proteomes of nacre and prismatic layer of the marine gastropod Haliotis laevigata were analyzed combining mass spectrometry-based proteomics and next generation sequencing.
We identified 297 proteins from the nacreous shell layer and 350 proteins from the prismatic shell layer from the green lip abalone H. laevigata. Considering the overlap between the two sets we identified a total of 448 proteins. Fifty-one nacre proteins and 43 prismatic layer proteins were defined as major proteins based on their abundance at more than 0.2% of the total. The remaining proteins occurred at low abundance and may not play any significant role in shell fabrication. The overlap of major proteins between the two shell layers was 17, amounting to a total of 77 major proteins.
The H. laevigata shell proteome shares moderate sequence similarity at the protein level with other gastropod, bivalve and more distantly related invertebrate biomineralising proteomes. Features conserved in H. laevigata and other molluscan shell proteomes include short repetitive sequences of low complexity predicted to lack intrinsic three-dimensional structure, and domains such as tyrosinase, chitin-binding, and carbonic anhydrase. This catalogue of H. laevigata shell proteins represents the most comprehensive for a haliotid and should support future efforts to elucidate the molecular mechanisms of shell assembly.
Species of the gastropod genus Haliotis construct a shell with two clearly distinguishable major layers, prismatic and nacreous, both of which are a composite of mineralized CaCO3 and organic molecules [1, 2]. The outer, relatively soft and chalky prismatic layer is comprised of prism-shaped crystals. The inner mother-of-pearl layer, or nacre, is characterized by thin intercalated plates and has attracted much more interest as a model in biomaterials and biomineralization research than the prismatic layer. This is due to its extraordinary toughness and fracture resistance conferred by the arrangement of individual aragonite crystals which are connected by mineral bridges and enclosed by a thin layer of organic matrix [3,4,5,6].
In both layers the crystals are enveloped and pervaded by an organic matrix that constitutes approximately 2% of the total bio-composite weight, and which is composed predominantly of protein and polysaccharide. The mineral and organic precursors of the shell are secreted by the mantle epithelium that lines the extrapallial space between mantle tissue and the shell . The secreted organic matrix is thought to assemble extracellularly and to provide a mold that templates and guides the growth of the mineral . In fact isolated H. rufescens organic shell matrix was shown to control nucleation, crystal orientation, the nature of the calcium carbonate polymorph deposited [8,9,10,11], and to act as an adhesive between the aragonitic plates .
The search for individual proteins responsible for these effects by molecular biological and biochemical methods lead to the discovery in H. rufescens nacre of lustrin A, a large multi-domain protein  that is localised immunohistochemically to the extra-crystalline matrix between nacre plates . Other Haliotis proteins isolated and characterized include the mineral-binding C-type lectin perlucin [14, 15], the IGF-binding protein perlustrin , the mineral-binding proteins AP7 and AP24 , the crystal morphology-modifying AP8 proteins , the crystal growth-inhibitor perlwapin , and perlinhibins, low-abundance Cys-, His- and Arg-rich mini-proteins that inhibit calcium carbonate crystallization . More recently increased application of mass spectrometry-based proteomic techniques to biomineral matrices has enabled the identification of comparatively large numbers of proteins in a short time without the need to resort to complicated protein separation protocols. However, for these proteomic methods one still requires sequence databases as comprehensive as possible to obtain meaningful results. Examples of the application of such proteomic methods to haliotids with relatively limited EST databases created by Sanger sequencing include analyses of the shell organic matrix in H. asinina  and H. tuberculata . Altogether 21 proteins were identified by searching mass spectra against translated EST sequences of H. asinina. Perlwapin was the only protein among these 21 that had been previously identified. The study on H. asinina  compared the proteomes of the entire shell and nacre alone. Five proteins were identified in the whole shell but not in nacre, indicating that they were restricted to the prismatic layer and may induce the formation of prisms or the inhibition of nacre. Similarly, differences in protein composition were also found in more comprehensive studies of separate shell layers of the pearl oysters Pinctada margaritifera and P. maxima  and various Mytilus species [24, 25].
Next generation sequencing (NGS) techniques have developed rapidly and allow for the rapid sequencing of entire genomes and transcriptomes that can be used to study not only the expression of biomineralization-related genes, but also as sequence databases for more comprehensive proteomic studies. In the present report we have conducted an in-depth proteomic analysis of the separated prismatic and nacreous layer organic matrices of H. laevigata coupled with transcriptomic sequencing of Haliotis mantle tissue. The resulting shell-associated proteome included almost all previously identified Haliotis proteins as well as many new proteins that were annotated with respect to abundance, similarity to other proteins, predicted domain structure, predicted secretion signal peptide and transmembrane segments, isoelectric point, amino acid composition, and predicted intrinsic disorder. We have also compared these proteins with similarly derived datasets from a range of other molluscs and more distantly related invertebrates in order to determine what broad level of sequence similarity exists between these biomineralising proteomes.
Preparation of matrix and peptides
Haliotis laevigata shells of lengths of 15-18 cm and weights of 150-200 g were treated with a final concentration of 4% sodium hypochlorite solution (Carl Roth, Karlsruhe, Germany) for 2 h without (method A) or with (method B) a 5 min ultrasound treatment at the start of each hour. Shells were then washed extensively with deionized water and dried. Alternatively, the nacreous layer of a shell not washed with hypochlorite before was sand-blasted from each side to remove possible contaminants (method C). Nacre matrix was prepared as described previously . For prismatic shell layer preparation the surface of shells was cleaned mechanically to remove mineralized worm tubes and other material not belonging to the shell. Shells were then washed with hypochlorite as before (methods A and B) and the prismatic shell layer was filed off and collected for demineralization. Calcite powder and nacre pieces were dissolved in 12% acetic acid and the suspension was dialyzed and stored in 3% acetic acid at 4 °C for 13 days until centrifugation. Acid-soluble and acid-insoluble matrix components were separated by ultracentrifugation (Optima LE 80 K, 45Ti rotor, Beckman Coulter, Krefeld, Germany) at 4 °C and 146,900 x g for 60 min. The fractions were then lyophilized for concentration and storage. Matrix proteins were separated by SDS-PAGE in pre-cast 4–12% Novex Bis-Tris gels using the MES buffer system with reagents and protocols supplied by the manufacturer (Invitrogen, Carlsbad, CA) except for the reducing agent, which was β-mercaptoethanol added to a final concentration of 2%. The sample buffer contained lithium dodecyl sulphate (LDS, final concentration 1%) while pre-cast gels and running buffer contained SDS (0.1%). Samples were suspended in 30 μl sample buffer/200 μg of organic matrix, boiled for 5 min, and centrifuged at 13000 rpm for 5 min in an Eppendorf bench-top centrifuge before SDS-PAGE analysis. Separated proteins were stained with colloidal Coomassie blue (Invitrogen). Gels containing acid-soluble nacre matrix and acid-insoluble prismatic layer matrix were cut into 12 slices and identical slices of three lanes were used for in-gel digestion with trypsin . All slices were treated equally irrespective of staining intensity or presence of visible bands. The eluted peptides were cleaned with C18 Stage Tips before MS analysis . The acid-soluble fraction of the prismatic layer and the acid-insoluble matrix of nacre, PAGE analysis of which showed no or only few and week protein bands, respectively, were cleaved using a filter-aided sample preparation (FASP) method [29, 30] modified as follows. Matrix components were dissolved in 0.1 M Tris buffer, pH 8, containing 6 M guanidine and 0.01 M dithiothreitol (DTT) and heated to 56 °C for 60 min. Aliquots containing 200, 400 and 800 μg of matrix were then loaded onto Microcon YM-30 centrifugal filter devices (Millipore) and DTT was removed by centrifugation at 13000 rpm in a Eppendorf bench top centrifuge model 5415D for 10 min and washing with 2 x 1vol of the same buffer. Carbamidomethylation was performed in the device using Tris-guanidine buffer containing 0.05 mM iodoacetamide and incubation for 45 min in the dark. Carbamidomethylated proteins were washed with 0.05 M ammonium hydrogen carbonate buffer, pH 8, containing 2 M urea, and centrifugation as before. Trypsin (2 μg, Sequencing grade, modified; Promega, Madison, USA) was added in 40 μl of the same buffer and the devices were incubated at 37 °C for 16 h. Peptides were collected by centrifugation and the filters were washed twice with 40 μl of buffer. The peptide solution was acidified to pH 1–2 with trifluoroacetic acid and peptides were cleaned and concentrated using C18 Stage Tips .
LC-MS and MS data analysis and transcriptomics
Peptide mixtures were fractionated by on-line nanoflow liquid chromatography using the EASY-nLC 1000 system (Thermo Fisher Scientific, Germany) with 20 cm capillary columns of an internal diameter of 75 μm and filled with 1.8 μm Reprosil-Pur C18-AQ resin (Dr. Maisch GmbH, Ammerbuch-Entringen, Germany). Column temperature was 30 °C. The gradient consisted of 5–30% buffer B (80% acetonitrile in 0.1% formic acid) for 85 min, 30–60% buffer B for 12 min and 60–80% buffer B for 7 min at a flow rate of 250 nl/min. The eluate was electrosprayed into an LTQ Orbitrap Velos or Orbitrap Elite (Thermo Fisher Scientific, Germany) through a Proxeon nanoelectrospray ion source. The Orbitrap Velos and Orbitrap Elite were operated in a HCD top 10 mode essentially as described ((Velos), (Elite)). Survey full scan spectra (from m/z 300–1750) were acquired at a resolution of 30,000 (Velos) and 120,000 (Elite) at m/z 400. Dynamic exclusion time was 90s. Raw files were processed using version 184.108.40.206 of MaxQuant [33,34,35,36] a computational proteomics platform based on the Andromeda search engine (http://www.coxdocs.org/doku.php?id=maxquant:start) . The protein databases used for protein identification were derived from H. laevigata hemolymph and epipodial tentacle tissue  and mantle tissue (see below). The hemolymph and tentatacle database was kindly provided by Dr. Shiel (Department of Genetics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne) in the form of a nucleotide database that we translated into protein sequences using the EMBOSS Transeq program (http://www.ebi.ac.uk/Tools/st/emboss_transeq/)  with six reading frame translation, trim option and the standard code. Because this transcriptomic database has not yet been deposited in a publicly accessible database, we have compiled accessions confirmed by peptide MS/MS sequences in Additional file 1. This file contains the sequence with the most peptide matches occurring in the respective MaxQuant output table protein group. In addition we generated a new mantle tissue transcriptome for what turned out in retrospect to apparently be a hybrid species between H. laevigata and H. rubra. Briefly, the mantle tissue from an animal collected from Ocean Wave Seafoods (Lara, Victoria, Australia) was dissected and total RNA extracted using TriReagent according to the manufacturer’s instructions. Total RNA was used for Illumina library preparation and 100 bp paired end stranded sequencing on the HiSeq2000 platform. We collected more than 137 million reads which have been deposited in GenBank under SRP126753. Trimmomatic  was used to remove low quality reads and adapter sequences. Reads were assembled de novo using our recently developed assembly pipeline . Briefly, we employed three assembly packages with unique assembly strategies: Trinity V2.0.3 , the commercial CLC Genomics Workbench and IDBA-tran V1.1.1 . This transcriptome assembly was complemented by a Haliotis sequence subset of the UniProt protein sequence database (release 1015–06; 1404 entries with Haliotis as organism). Databases were combined with the reversed sequences and sequences of widespread contaminants, such as human keratins. Carbamidomethylation was set as fixed modification. Variable modifications were methionine oxidation, N-acetyl (protein), pyro-Glu/Gln (N-term) and phosphorylation (S,T,Y). Maximal peptide mass tolerance was set to 20 ppm and 6 ppm for first search and main search, respectively. MS/MS mass tolerance was set to a maximal value of 20 ppm. Two missed cleavages were allowed and the minimal length required for a peptide was seven amino acids. Maximal FDR for peptide spectral match, proteins and site was set to 0.01. The minimal score for modified and unmodified peptides was 60. Identifications with only two sequence-unique peptides were routinely validated with the help of the MaxQuant Expert System software of MaxQuant  considering the assignment of major peaks, occurrence of uninterrupted y- or b-ion series of at least four consecutive amino acids, preferred cleavages N-terminal to proline bonds, the possible presence of a2/b2 ion pairs, immonium ions and mass accuracy. Only identifications with at least two peptides in a preparation and occurring in at least two preparations of the same shell layer were accepted. Identifications with only one sequence-unique peptide or only in one fraction were exceptionally accepted if only one measurable peptide was predicted under regular cleavage conditions or if it shared peptides with other proteins. The iBAQ (intensity-based absolute quantification)  option of MaxQuant was used to calculate, based on the sum of peak intensities, the approximate share of each protein in the total proteome, including identifications that were not accepted finally. The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE  partner repository (https://www.ebi.ac.uk/pride/archive/) with the dataset identifier PXD009567.
Other bioinformatics analyses
Protein similarity searches were performed using FASTA (http://www.ebi.ac.uk/Tools/sss/fasta/)  against the UniProt Knowledgebase. Some published sequences not in public protein databases were searched against H. laevigata sequences using the Local Blast function  of BioEdit Sequence Alignment Editor v.7.2.5 (http://www.mbio.ncsu.edu/bioedit/bioedit.html). Domain prediction including prediction of signal peptides and transmembrane segments was done with InterProScan (http://www.ebi.ac.uk/interpro/search/sequence-search) . Signal peptide prediction was confirmed using SignalP 4.1 (http://www.cbs.dtu.dk/services/SignalP/) . Intrinsically disordered proteins (IDP) and intrinsically disordered regions (IDR) were predicted with MFDp2 [49,50,51] (http://biomine.cs.vcu.edu/servers/MFDp2/). Sequence alignments were done with the help of Clustal Omega (http://www.ebi.ac.uk/Tools/msa/clustalo/) . Amino acid composition and isoelectric point of protein sequences were calculated using the ExPasy tool ProtParam (http://web.expasy.org/protparam/) after removal of predicted signal peptide sequences . Venn diagrams were drawn using Venn Diagram Plotter (https://omics.pnl.gov/software/venn-diagram-plotter). Some sequences were analysed for tandem repeats using XSTREAM (http://jimcooperlab.mcdb.ucsb.edu/ xstream/) . In some cases the results were checked with PrDOS  (http://prdos.hgc.jp/cgi-bin/top.cgi) and IUPred  (http://iupred.enzim.hu/pred.php). BLASTp sequence similarity comparisons of the 77 major H. laevigata shell proteins described in Table 1 (and in addition 3 contigs encoding UP6 and UP7 as described in ) were performed against a variety of calcifying proteome datasets derived from a wide phylogenetic range of metazoans as described in . These included: 42 proteins from the oyster Pinctada maxima reported in ; 78 proteins from the oyster Pinctada margaritifera reported in ; 94 proteins from the abalone Haliotis asinina reported in [21, 57]; 63 protein from the limpet Lottia gigantea reported in ; 53 proteins from the oyster Crassostrea gigas reported in ; 71 proteins from the mussel Mya truncata reported in ; 59 proteins from the grove snail Cepaea nemoralis reported in ; 44 proteins from the oyster Pinctada fucata reported in ; 53 proteins from the mussel Mytilus coruscus reported in ; 66 proteins from the brachiopod Magellania venosa reported in ; 139 proteins from the sea urchin Strongylocentrotus purpuratus reported in ; 37 proteins from the coral Acropora millepora reported in . A consensus phylogenetic tree was manually constructed for all of these species based on a selection of previous studies [65,66,67,68].
Results and discussion
Isolation of biomineralized organic matrices
In the literature different protocols can be found that differ in the length of hypochlorite treatment used to clean the biomineral prior to extraction of organic molecules. Here we cleaned most H. laevigata shells with sodium hypochlorite prior demineralization to destroy and remove contaminating organic material adhering to the shell surface. However, a treatment lasting 24 h as previously reported  visibly damages the nacreous part of the Haliotis laevigata shell. Apparently some nacre tablets were detached from the shell and the shell lost some of its lustre and took on a whitish, opaque appearance at the rim. We ascribed this to the partial destruction of the extra-crystalline matrix encasing the typical aragonite tablets of nacre. Therefore the hypochlorite treatment was limited to 2 h (method A) and was combined with short periods of ultrasound treatment with one shell (method B). Possibly different shell types respond differently to hypochlorite treatment, because we did not observe visible damage after 24 h treatment of complete Lottia gigantea shells and also did not find major differences in the proteomes extracted after 2 h or 24 h washing . One shell was not treated with hypochlorite at all, but the nacreous layer was sand-blasted from both sides to remove the prismatic layer and upper nacreous layers to obtain pure nacre without any chemical treatment (method C). However, this was not possible with the prismatic layer because it is much thinner and softer than nacre. Therefore only methods A and B were used for the preparation of the prismatic layer. Traditionally the organic shell matrix is separated into acid-soluble and acid-insoluble fractions by centrifugation, and we followed this protocol. Acid-soluble matrix yields were 2-3 mg/g of shell for nacre and 3-7 mg/g for the prismatic layer (Additional file 2: Table S1). Minor, mostly quantitative, differences observed between the SDS-PAGE protein band patterns (Additional file 3: Figure S1) of shell matrices extracted from shells after different cleaning protocols may be due to unintentional technical variations. In contrast, matrices isolated from the different shell layers, nacreous or prismatic, showed very different protein band patterns (Fig. 1 and Additional file 3: Figure S1). Furthermore, we also observed differences between acid-soluble and acid–insoluble fractions (Fig. 1). Differences between nacre acid-soluble and acid-insoluble fractions seemed to be mostly quantitative, while differences between respective prismatic layer fractions were quite dramatic (Fig. 1). Although the yield of matrix in the prismatic layer acid soluble-fraction was much higher than in the acid-insoluble fraction, almost no protein was observed in this fraction indicating that most of the matrix was either not protein or not visible with Coomassie Blue stain (Fig. 1) nor additional silver staining (not shown), or alternatively was not soluble in the denaturing PAGE sample loading buffer. In fact centrifugation of samples after solubilization in PAGE sample buffer produced large insoluble pellets. The recalcitrant nature of many biomineral-associated proteins to standard chromatographic and electrophoretic techniques is well recognized  and likely also contributes to the discrepancy we see between acid-soluble and acid-insoluble fractions of the prismatic layer. Acid-soluble fractions of nacre matrix and acid-insoluble fractions of the prismatic layer were separated by SDS-PAGE and in-gel digested. The nacre acid-insoluble matrix and the prismatic layer acid-soluble matrix, which seemed to be less important (as to protein content) were digested in solution using a filter-aided sample preparation (FASP, [29, 30]) technique. All in-gel digested samples were analysed with three technical replicates resulting in a total of 36 raw-files per fraction that were run together in MaxQuant. The in-solution samples were run with five replicates resulting in five raw-files per fraction.
Comparison of nacre and prismatic layer proteomes
Applying the criteria for acceptance of identifications detailed above in Materials and methods almost 450 proteins were identified (Additional file 4: Table S2; Additional file 5: Table S3). The distribution of proteins between the different fractions obtained with different shell purification methods is shown in Fig. 2. All identifications including those not accepted, for instance single peptide identifications, were retained in the respective MaxQuant output files shown in Additional files 6, 7, 8, 9, 10, 11, 12, 13, 14, and 15 for protein groups. Additional file 16 shows the distribution of nacre and prismatic layer proteins among gel slices. Additional files 17, 18, 19, 20, 21, 22, 23, 24, 25, and 26 show the corresponding identified peptide data f. The numbers of proteins in Fig. 2 and Additional file 4: Tables S2 and Additional file 5: Table S3 should be considered tentative. Thus, some database entries may contain the sequences of several distinct proteins while others may contain only partial sequences of the same protein. We have tentatively combined such fragments into one group as indicated by the differential shading in Additional file 4: Tables S2 and Additional file 5: Table S3. Other proteins have very similar sequences and share most of their peptides. One example of this is the perlucin splice variants detected by cDNA cloning . Because of the sequence similarity and therefore high number of shared peptides we were not able to disentangle and properly quantify the different peptide sets and therefore chose to count these variants as one group. Finally, some proteins may have been missed because of their low abundance, such as perlinhibin and perlinhibin-related protein . These mini-proteins were observed to occur at a very low concentration and their abundance may be too low to be detectable in such a proteomic survey without prior enrichment. Other reasons for missing proteins may be an absence of the respective sequence from the nucleotide databases, or a lack of trypsin cleavage sites. In general, the nacre samples extracted after sodium hypochlorite treatment yielded more proteins and peptides than the samples from shells that were mechanically cleaned, indicating that hypochlorite washing in some way facilitated protein extraction. However, the differences in proteomic results from shells cleaned with different methods were not considered to be meaningful enough to be explored further. Instead we aimed at obtaining a representative shell proteome of H. laevigata. As expected from SDS-PAGE results, most of the proteins isolated from nacre without chemical cleaning were found in acid-insoluble fractions (Fig. 2a). With prismatic layer samples, most proteins were identified in the acid-insoluble samples. In fact no protein was identified exclusively in the acid-soluble fractions (Fig.2b).
As previously described , we used MaxQuant iBAQ [35, 72] to discern minor and major proteins. The peptide yield of the previously localized extra-crystalline matrix protein lustrin A [12, 13], predominantly identified in the acid-insoluble fractions of nacre, was not particularly affected when the shell was treated with sodium hypochlorite (Additional file 4: Table S2), indicating that our relatively mild washing most probably not did destroy the extra-crystalline matrix to an appreciable extent. We assume that the major proteins are likely to play an important role in shell assembly and shell structure, although minor proteins may of course be important for shell assembly by virtue of enzymatic activities or as part of a signaling network. In the following section we will focus our discussion on the quantitatively major proteins from both H. laevigata shell layers (Table 1).
Major proteins of the H. laevigata shell
For the present report we defined major proteins as those that occur in at least two different preparations with an abundance of ≥ 0.2% of the total. However, we did not count those proteins with ≥ 0.2% occurring exclusively in prismatic layer acid-soluble samples, because these samples yielded only very few proteins and apparently did not contain much protein at all (see above) and therefore most likely do not matter quantitatively. In this way we obtained a total of 77 major proteins. This group contained almost all of the proteins previously identified in Haliotis shells (Table 1) with the obvious exceptions of UP6_HALAI and UP7_HALAI previously identified in H. asinina , the H. laevigata homologs of which were identified as minor proteins in the prismatic layer and in nacre, respectively (Additional file 4: Table S2; Additional file 5: Table S3). Of the 77 major proteins 34 were categorized as major exclusively in nacre samples and 26 exclusively in prismatic layer samples. Seventeen proteins occurred with the required abundance of ≥ 0.2% in samples from both layers (Fig.2c, right). However, most of the major proteins (86%) could be identified as occurring in both nacre and prismatic layers, but frequently as a minor protein in one of the layers. Only 11 major proteins were identified exclusively in either nacre or prismatic layer (Table 1). One unexpected shell-associated protein was actin with abundances in three fractions just above our threshold for definition as major protein (> 0.2%; Table 1). Cytoskeletal and intracellular housekeeping proteins are frequently identified in biomineral proteomes, and many others than actin also occurred as minor proteins in the proteome of H. laevigata (Additional file 4: Tables S2 and Additional file 5: Table S3). When such proteins are identified in shells they are commonly considered to be contaminants as their presence in the shell matrix is difficult to reconcile with current models of shell matrix assembly. We took great care in cleaning the surface of the shells before extraction of the matrix, indicating that these proteins were an integral part of the shell structure and are difficult or impossible to remove without causing damage. This was also shown to be the case with the shell of the brachiopod Magellania venosa , where we succeeded in significantly reducing the level of intracellular proteins when we treated powdered shell particles for 24 h with hypochlorite, but also lost some interesting proteins with some features characteristic of shell proteins, probably by removal of a large part of the extra-crystalline matrix. In mammals, intracellular proteins like the cytoskeletal component actin have been found at the cell surface, in extracellular matrices, and in body fluids (reviewed in ). The source of these proteins remains essentially unknown, but one suspected origin is from damaged or stressed cells. Currently it remains unknown whether such proteins are inadvertently occluded into the growing edge of the biomineral, or whether they genuinely play a functional role in biomineralisation. One piece of information that links the cytoskeleton to the process of shell formation comes from an unusual chitin synthase gene isolated from the marine bivalve Atrina rigida  that contains a myosin head domain that may interact with the actin cytoskeleton, thus providing a link between a component of the shell-forming machinery and the cytoskeleton .
Nacreous and prismatic layers have been separately analyzed in species other than Haliotis previously. The shell of the pearl oyster Pinctada  yielded a total of 80 identified proteins. Forty-seven of these were apparently prism specific and 30 were nacre specific. Only three were identified in both compartments. More overlap was found in the different compartments of Mytilus shells. Nacre, fibrous prism and myostracum layers of M. coruscus  yielded a total of 63 proteins with 16 nacre specific proteins, 14 fibrous prism specific proteins, and eight myostracum specific proteins. Twelve proteins were shared by all three compartments, eight by nacre and myostracum, and five by nacre and fibrous prism layers. Mytilus galloprovincialis provided similar distributions with a total of 113 identified proteins . The total numbers of identified proteins were similar to the number of major proteins we identify in the present report. However, no abundance estimates were provided for Pinctada or Mytilus proteins.
The list of major proteins contains some very acidic proteins and many proteins predicted to contain intrinsically disordered regions (IDR) or to be intrinsically disordered proteins (IDP) altogether. Both properties are thought to play an important functional role and have attracted much attention. Some of the first characterized proteins of biomineral organic matrices were unusually acidic with calculated isoelectric points close to four due to a high proportion of aspartic acid in their sequences. Early examples include MSP-1 from the shell of the scallop Patinopecten yessoensis [76, 77], prismalin-14 from the prismatic layer of the oyster Pinctada fucata , and aspein also from Pinctada fucata . Because of their possible ability to bind calcium ions in solution and on crystal surfaces by electrostatic interaction, acidic proteins were suggested to control crystal nucleation or crystal growth regulation  and became a major topic of biomineralization research . However, it soon became apparent that biomineral matrices did not only contain acidic proteins but also neutral and basic ones . Furthermore, many of these proteins displayed biased amino acid compositions with high percentages of certain amino acids, most often Ala, Gly, Gln, Ser and Pro. Frequently these amino acids occurred in uninterrupted blocks or in short repetitive sequence stretches . An early example of such a shell protein was MSI60 from the oyster Pinctada fucata that consisted to 26% of Ala and 37% of Gly . Biomineral matrix proteins with large stretches of simple repeats comprise, for instance, nacrein of the gastropod Turbo marmoratus , or pearlin from Pinctada margeritifera  that contain extended blocks of Gly-Asn repeats. Proteins or protein regions with such characteristics frequently do not have a three-dimensional structure under native conditions and belong to the widespread group of intrinsically disordered proteins [87,88,89]. IDPs and IDRs apparently also occur frequently in biomineral matrix proteins [90,91,92] therefore prediction of disorder was added to the annotations in Additional file 4: Tables S2 and Additional file 5: Table S3.
Major proteins previously known as Haliotis shell components
Most of the proteins previously identified in Haliotis shells were identified in this proteomic survey above the threshold set for major proteins. The H. laevigata C-type lectin perlucin  and the WAP domain–containing perlwapin  were among the most abundant proteins of the nacreous layer (Table 1). Both proteins were shown to modulate calcium carbonate nucleation and crystal growth in vitro [15, 19, 93]. Perlucin was recently shown to occur in several splice variants . In this survey we indeed found evidence for several perlucins (Additional file 4: Table S2; more than 60 when we perform a tBLASTn search against the assembled transcriptome). However, the sequences of these variants were so similar that most of them shared most of their peptides and we were not able to quantify them properly. Consequently they were treated as one protein in this report. The small H. laevigata nacre IGF-binding protein perlustrin  was found with lower and variable abundance (Table 1). Interestingly, the H. laevigata shell contained another very similar protein (about 70% identical to PLS_HALLA in overlapping sequence regions; Additional file 4: Table S2; Fig. 3), which was found in the tentacle/hemolymph-derived database  and was identified as a major protein in both, nacre and prismatic layer. These perlustrins did not share peptides, but each amino acid sequence was validated by proper MS/MS-sequences (Fig. 3). Interestingly, hemocytes were previously shown to contribute to shell mineralization and repair in Crassostrea virginica and Pinctada fucata [94, 95] and to be present in the extrapallial fluid .
Fragments of the long extra-crystalline matrix protein lustrin A were identified in several transcriptome database entries (Additional file 4: Table S2). The leading entries CLC_1320, Tri_116352, idb_288 and CLC_608 were on average 74% identical to H. rufescens (O44341_HALRU; ) and H. tuberculata (A0A088CBA1_HALTU, F6KD05_HALTU; ) sequences and covered approximately 70% of the sequence of O44341_HALRU, apparently the most complete lustrin A. In agreement with this we previously reported great difficulty in assembling a complete lustrin from NGS data, most probably due to the repetitive architecture of this protein .
Entry Tri_24151 possibly contained the sequence of a H. laevigata counterpart of H. rufescens AP7  (Fig. 4). H. rufescens AP7 (Q9BP37_HALRU) was shown to consist of two small domains, a calcium-binding N-terminus [17, 97] following the secretion signal peptide, and a C-terminal C-RING-like domain , which was found to participate in in vitro protein-protein interactions, self-assembly, and mineral nucleation [99, 100]. The sequence identity of Tri_24151 to Q9BP37_HALRU was only 43.5% and the e-value (0.0005) was relatively high (Additional file 4: Table S2). The four cysteines probably taking part in multivalent metal ion binding  were preserved in the H. laevigata sequence (Fig. 4). However the N-terminal domain of AP7 was disrupted in Tri_24151 by a 58aa-long insertion. The predicted N-terminus of the mature protein, the insert, the N-terminal domain and the C-terminal domain of the presumptive translation product were confirmed by MS/MS-derived peptide sequences (Fig. 4). AP7 was shown to be at least partially disordered , a feature that was not predicted for Tri_24151 by neither MFDp2 nor two other disorder prediction programs (IUPred and PrDos). Protein Tri_24151 was identified with very high abundance (> 1.0%) in samples of hypochlorite-treated nacre, with lower abundance in untreated nacre and even less in prismatic layer samples (Table 1). In the original report the column fraction containing AP7 contained another nacre protein, AP24 . A very similar protein (77.8% identity; Additional file 4: Table S2) was contained in entry CLC_1642. As for the N-terminal 30aa of AP7, the N-terminus of AP24 was shown by NMR to be disordered , but again this feature was not predicted by the prediction software programs we used. Instead, the region between aa152–176 was predicted to be disordered. AP24 was identified in nacre, but at a much lower abundance than AP7 (Table 1).
The first proteomic analyses of Haliotis shell matrices [21, 22] yielded 17 and 7 proteins, respectively, including perlwapin and three tentatively identified proteins. The H. asinina shell  contained seven proteins essentially without predicted domain structure, the recommended name of which in the UniProtKB database is uncharacterized protein (UP) 1 to 7. In the present report we will also use this name (Tables 1, Additional file 4: Table S2 and Additional file 5: Table S3). UP3 (CLC_39) and UP4 (Tri_119193) were among the most abundant proteins in nacre with abundances of > 1.0% in all nacre samples (Table 1). UP1 (Tri_1743) was a major protein in all prismatic layer samples (Table 1). UP2 (idb_34528) and UP5 (idb_50885/18771/18767) were less abundant, but still major proteins predominantly identified in nacre. UP6 (idb_59441 and idb_27788) and UP7 (Tri_100716) did not comply with our thresholds for major proteins but were identified and classified as minor proteins (see below). The average sequence identitity between H. asinina UPs and their H. lavigata equivalents was 80–81%.
Another important group of H. asinina prismatic layer matrix components were two ependymin-related proteins, EDPR 1 (ML1E6) and EDPR 2 (6G3) . In H. laevigata we identified many entries containing predicted ependidym domains (Additional file 4: Table S2, Additional file 5: Table S3), many of them sharing peptides. The table of major proteins (Table 1) contains nine ependymin-related entries. Besides shared peptides many of them contained sequence unique peptides often located at identical positions of alignments to EDPR 1 and 2. From our data it was difficult to decide whether these were independent but related gene products or variants of a particular protein. The entries most similar to the H. asinina  proteins were Tri_31892 for EDPR1 with 84.3% identity and CLC_1876 for EDPR2 with 64.0% identity. However, in FASTA searches against the UniProtKB database EDPR1 was the highest scoring match in both cases. The best match for EDPR2 in FASTA searches was idb_52687 with 57.6% identity (Additional file 5: Table S3). As reported for EDPR1 and 2 in H. asinina , these proteins were most abundant in prismatic layer samples and were either not identified not at all or only in negligible amounts in nacre. The only exception was Tri_31892/comp22593_c0_seq1_3 that was also a major protein in nacre (Table 1). Tri_31892 was also similar to an ependymin-like protein extracted from the nacre organic matrix of H. diversicolor (AEP 25 kDa; ).
Other major proteins previously identified in the shell of H.asinina  were KCP_HALAI (P0012N13_463), GAAP_HALAI (HasCL10contig2), QRP_HALAI (ML8B1), and DGRP_HALAI (P0025F23_658), which were also among the major proteins of the H. laevigata shell matrix (Table 1). Sequences with approximately 83% sequence identity to the BPTI/Kunitz domain-containing protein KCP were identified in CLC_148, CLC_77 and Comp84928_c0_seq1_4. Despite some sequence differences confirmed in part by MS/MS-sequenced peptides (Additional file 4: Table S2) these proteins were so similar to each other and KCP that we chose to treat them as variants of one protein (Fig. 5), and were identified as major proteins in both shell layers. However, as in all such cases encountered, these entries could of course also represent different gene products. Glycine-, alanine- and asparagine-rich protein (GAAP) was contained in H. laevigata sequence database entries Tri_107535/CLC_21 with 77.5% sequence identity. This protein was also identified as a major protein in both shell layers (Table 1). A sequence with 57.1% identity to glutamine-rich protein (QRP_HALAI) was identified in the C-terminal half of entry CLC_253 (Additional file 27: Figure S2D). In contrast to  we identified this protein only in the acid-insoluble fractions of nacre. Possibly this difference was due to different centrifugation procedures. While we used ultracentrifugation, Marie et al.  used centrifugation at 3900 g to sediment acid-insoluble matrix. However, sedimentation by ultracentrifugation would require some kind of aggregation with itself or other matrix components. A protein with 73.9% identity to aspartate- and glycine-rich protein of H. asinina (DGRP_HALAI) was detected in the C-terminal half of entry Tri_57798 (Additional file 4: Table S2). The N-terminal half of this entry was most similar to part of the MSI60-related protein of Pinctada fucata (46.4% identity to G9MD31_PINFU; ) and the entire entry was 32.2% identical to molluscan shell protein 1 (MSP-1) of Mizuhopecten yessoensis (Q95YF6_MIZYE; [76, 77]). Of the tentatively (with a single unique peptide) identified proteins of Marie et al. , ML3D4 was similar to Tri_25106 and idb_20988 (Table 1, Additional file 4: Table S2). These in turn were similar to a putative amine oxidase identified in the shell proteome of Mytilus coruscus (A0A0G2YN89_MYTCO; ).
A pilot study of the H. tuberculata shell proteome  contained four new proteins not identified in Haliotis shells before. The protein similar to hasinaP0014F12_631 was similar to aa615–745 of entry CLC_303 (Table 1, Additional file 4: Table S2), similar to ML7B12 was similar to Tri_63049 (Table 1, Additional file 4: Table S2), similar to hasinaP008C13_381 was similar to aa94–216 of Tri_57798 (Table 1, Additional file 4: Table S2), and similar to ML7A11 was similar to aa24–244 of Tri_11338 (Table 1, Additional file 4: Table S2).
Major proteins previously detected in transcriptomic studies of Haliotis mantle tissue
Carbonic anhydrases (CA) catalyze the formation of hydrogen carbonate from CO2 and H2O. This is an extremely important reaction for calcium carbonate biomineral-forming organisms and the enzyme(s) are therefore almost ubiquitous . Many molluscs produce α-carbonic anhydrases in the mantle tissue and often these enzymes are recovered from biomineral matrices, for instance in Lottia gigantea [69, 105]. To date no carbonic anhydrase protein has been identified in a haliotid although mRNAs coding for two predicted CAs were identified in the mantle transcriptome of Haliotis tuberculata . However, proteomic analysis and enzyme activity assays failed to reveal the presence of carbonic anhydrase in the matrix . One of the putative α-CA proteins was predicted to be a secreted protein (htCA1), the second one was predicted to be a transmembrane protein (htCA2) . We have identified two CAs among the major proteins of Haliotis laevigata shell matrix (Table 1). One of them, Tri_72839, was present predominantly in acid-insoluble nacre samples while the second one, Tri_130845/idb_813, was present almost exclusively in acid-insoluble prismatic layer samples. Both were predicted to be secreted (Table 1, Additional file 4: Table S2, Additional file 5: Table S3). The nacre enzyme, Tri_72839, was 78.5% identical to htCA2/G0YY03_HALTU of . The prismatic layer enzyme, Tri_130845/idb_813, was most similar to the Patella vulgaris putative CA (J7QJT8_PATVU; ), however only with 31.2% identity (Additional file 5: Table S3). No sequence similar to htCA1 was identified in the present study.
A glycine-rich putative secreted shell protein derived from the mantle transcriptome of H. asinina and termed glycine-rich boundary protein (A0A0B4VCR4_HALAI; submitted by McDougall C, Woodcroft B, Degnan B; 2014), was similar to Tri_17455 (Additional file 4: Table S2) and was not only rich in glycine but also in alanine, glutamine and methionine. About 64.6% of the sequence was predicted to be disordered. This protein was found to be one of the major H. laevigata nacre matrix proteins with an abundance > 1.0% in five out of six fractions (Table 1).
Major proteins not previously identified in Haliotis shell proteomes
The H. laevigata shell proteome also contained proteins not previously identified in Haliotis shells. However, these were predicted to contain domains or other features encountered previously in other mollusc shell proteins. Entries CLC_123/idb_32947 contained the sequence of a predicted tyrosinase. Messages coding for tyrosinase-like proteins have been detected in molluscan mantle transcriptomes and shells [108,109,110] and may be involved in shell protein cross-linking, especially in the periostracum. Tyrosinases may also play a role in shell coloration . In addition to the predicted tyrosinase domain in aa18–271, this entry also contained a short stretch of collagen triple-helical repeats in aa336–354 and the predicted disordered structure of the C-terminus consisted essentially of G-rich tandem repeats (Additional file 27: Figure S2B). Participation in cross-linking of matrix proteins has also been suggested for peroxidase-like proteins  identified in mollusc shell proteomes [56, 105]. The putative peroxidase contained in entry idb_25746 was a very abundant component of the acid-insoluble fractions of both the nacreous and prismatic layers (Table 1). The uncharacterized proteins with similarity to ferric-chelate reductase-like proteins in entries Tri_28544/Comp59223_c0_seq1_2 and Tri_61496 (Table 1) may also be involved in some kind of redox reaction important for shell protein cross-linking as suggested previously . The former contained a predicted DOMON domain typically found in dopamine β-monooxygenase/hydroxylase and a reelin domain. This protein was very abundant in acid-insoluble fractions of nacre while Tri_61496 was much less abundant and contained only a predicted reelin domain. Both proteins were predicted to contain disordered sequence regions (Additional file 4: Table S2). Mollusc shells are known to contain chitin, which contributes to the insoluble fraction of the shell matrix . Consequently most mollusc shell proteomes also contain proteins with chitin-binding and/or chitin-modifying domains. These proteins are likely to participate in chitin metabolism or to mediate between an insoluble chitin scaffold and functionally important soluble matrix proteins. The major proteins predicted to contain chitin-functionality (Table 1) were only a fraction of the total number of H. laevigata predicted chitin-binding shell matrix proteins identified (Additional file 4: Table S2 and Additional file 5: Table S3). CLC_4146/Comp87152_c0_seq1_4 was identified with very high abundance in the acid-insoluble prismatic layer samples while idb_25730/Comp68740_c0_seq1_1 was identified at a much lower abundance in nacre only. Both proteins contained in addition to the chitin-binding domain a von Willebrand A domain, a combination that is also known from shell matrix proteins Pif and BMSP [115,116,117].
More than half of the entries in the list of major proteins did not contain predicted domains. Frequently the respective protein sequences displayed biased amino acid compositions (Table 1) and the respective amino acids (frequently D, Q, A, S or P) were often organized in repetitive short motifs or longer sequence blocks of a few particular amino acids. Most of these proteins were predicted to be disordered and frequently they were very acidic. Repeats, together with their corresponding complete sequences are presented in Figure S2 (Additional file 27) and reference to sequences and their repeats is included into the second last column of Table 1. These kinds of distinctive features have also been observed in bivalve shell matrix proteins and other invertebrate biomineral matrix proteins [81, 82, 116, 118,119,120]. However, database searches with these uncharacterized H. laevigata proteins resulted either in no convincing match or matches based on particular amino acid composition features, such as extremely high aparagine or glycine content. This raises the question whether such proteins share true evolutionary homology. Previous comparisons between the mantle transcriptomes of the nacre-forming gastropod H. asinina and the nacre-forming bivalve Pinctada maxima indicated that proteins with such features, frequently called repetitive, low-complexity domains (RLCDs) are not related and are likely to be the result of convergent evolution . However, between species of one genus such proteins are thought to have evolved rapidly [120, 121]. The independent evolution of these proteins in different invertebrate classes implies that these sequences possibly embody common principles required for shell building. Table 1 contains several entries with very acidic isoelectric point (3.3–4.5). In all cases these sequences were predicted to be intrinsically disordered and contained tandem repeats of various lengths. However, only in two cases strongly acidic isoelectric point coincided with high concentration of aspartic acid (idb_22086 and Tri_57798, 36 and 25% D, respectively; Additional file 4: Table S2). Both proteins were still far away from such extreme aspartic acid accumulations as observed in bivalve aspein [79, 122] or asprich  with up to 75% aspartic acid. Entry Tri_57798 contained in the N-terminus an almost uninterrupted stretch of 55 aspartic acid residues, very much similar to the more extended D blocks in some bivalve proteins, in addition to short D-rich repeats (Additional file 27: Figure S2Zb). In idb_22086 and some related sequences aspartic acids were much more evenly distributed along the sequence and its repeats (Additional file 27: Figure S2K). Idb_22086 and 22,087 were identical up to aa309 and shared many peptides. The C-terminal sequences however were not related. In contrast, the N-terminal half of the much shorter sequence of idb_42421 aligned to a region in the C-terminus of idb_22086 (Additional file 27: Figure 2SK). The exact relationship between these three entries is not clear at present. The sequences could be those of distinct, but related proteins, or fragments of one or two proteins. All three contain many tandem repeats. For the time being we have preferred to put them into one group. A Q-rich protein other than the previously identified QRP (CLC_253) was contained in Tri_33510/CLC_62 (Additional file 27: Figure S2G). This very abundant nacre protein was predicted to be intrinsically disordered. The glutamines occurred in blocks of up to 10 Q in the C-terminal half of the sequence. The glutamine-, glycine- and proline-rich secreted intrinsically disordered prismatic layer protein of idb_20008 (Table 1) contained an almost uninterrupted sequence of 24 glutamines in aa80–104. In addition the sequence was full of short tandem sequence repeats of between 5 and 16 amino acids, the most numerous being 13 repeats of the type GMGNPM/TX in aa287–377 and some Q/P-rich repeats in aa470–573 (Additional file 27: Figure S2J). Other proteins contained stretches of very simple short repeats in tandem, such as [GN]n or [AQ]n. GN (or NG) tandem repeats as in CLC_4/Tri_11338 (Additional file 27: Figure S2E) and CLC_5/Tri_57798 (Additional file 27: Figure S2Zb), or related repeats, such as [GNN]n, were also found in the bivalve shell proteins nacrein , pearlin , N66 and N14 . Extended stretches of [AQ] and [AA] were found in CLC_303 (Additional file 27: Figure S2E) and idb_47306 (Additional file 27: Figure S2X). Proteins idb_54497/CLC_12027 contained in their predicted disordered region following the secretion signal peptide several G/M-rich repeats built around the motif [GMPG/MXn] (Additional file 27: Figure S2A). Overlapping sequences of entries CLC_73, idb_17035 and Tri_121458 (Additional file 27: Figure S2H) may be variants of one protein and were treated as such (Additional file 4: Table S2) although they also contained confirmed sequence-unique peptides at conflicting locations. However, all three entries also shared peptides and had very similar features as, for instance basic pI, high concentrations of serine, and predicted disordered structures. A distinctive feature of entry CLC_73 was a long N-terminal collagen triple-helical domain that was lacking in the shorter entries. This protein also contained in its sequence Ser-rich and tandem repeats. More sequences with tandem repeat structures are contained in Additional file 27: Figure S2 as cross-referenced in Table 1. All of these features are not new but occur identically or similarly in many other biomineralising proteins [91, 92, 125,126,127].
Minor proteins of potential importance
Although we assume that the most abundant proteins represent those of greatest functional significance, less abundant proteins can of course also have an impact if enzymatically active or form part of a signaling cascade. For this reason we focus on a few minor proteins of potential interest.
In addition to the major peroxidase-like idb_25746 we identified several other possible peroxidase/peroxidasin-like proteins which were contained in entries Comp51700_c0_seq3_3, idb_19812/idb_19814, and Tri_4200 (Additional file 4: Table S2 and Additional file 5: Table S3). Furthermore, entry idb_40380/Comp89520_c0_seq1_4 contained the sequence of a predicted superoxide dismutase. Superoxide dismutases are a family of enzymes with widespread subcellular distribution that remove superoxide, a normal aerobic metabolite that is also a substrate of peroxidases. Peroxidases have been implicated previously in mollusc shell formation . Possibly they are responsible for the sclerotization of the periostracum [128,129,130], the proteinaceous layer confining the mantle cavity before the start of mineralization. As discussed previously [21, 56] one may hypothesize that peroxidases function in stabilization of the newly secreted matrix by cross-linking some of its components. Although the highest scoring match in FASTA database searches for idb_19812 and idb_25746 was a Lottia gigantea sequence (Additional file 4: Table S2), this was not one of the peroxidases identified as major proteins in the L. gigantea shell. In addition to the major carbonic anhydrases in Tri_130845/idb_813 and Tri_72839 the H. laevigata shell prismatic layer contained several minor proteins predicted to be carbonic anhydrases because of their sequence similarity to other molluscan CAs and predicted CA domains. However, these proteins (Comp97413_c0_seq7_1/ idb_58049, Tri_119238, Tri_6552) were all of very low abundance (Additional file 5: Table S3). Metalloproteases, enzymes that were abundant in sea urchin biomineralized structures  were found predominantly in the insoluble fraction of the H. laevigata prismatic shell layer at low abundance (Additional file 5: Table S3; CLC_3466, idb_18707, idb_20328).
As briefly discussed above, chitin is a key component of mollusc shells. Thus all proteins and enzymes binding to chitin may be of potential importance for shell assembly. In addition to the major chitin-binding proteins in Table 1 we have identified many minor proteins predicted to bind chitin or related domains (summarized in Table 2). For most of these minor proteins the best matches, that is, the highest scoring hits appearing in the first line of the FASTP output, were molluscan proteins (Additional file 4: Table S2, Additional file 5: Table S3), the sequences of which were from genome sequencing projects of the limpet Lottia gigantea  and the oyster Crassostrea gigas . Rarely the sequences were from single gene cloning experiments, as for instance, the chitin metabolic enzyme genes of the freshwater mussel Hyriopsis cumingii (; J7FHX7 and J7F1C1, Additional file 4: Tables S2 and Additional file 5: Table S3), and even more rarely a protein was identified in a shell proteomic study, as for instance, PSM_MYTCA . The percentage of conserved residues between the species was rarely more than 40%.
Other minor proteins potentially important for shell assembly were the relatively abundant proteins similar to KCP in CLC_1047/Comp51373_c0_seq1_3 and the protein similar to shell matrix protein G9MBW9_PINMA (Tri_138845/ CLC_25186). The former was only 53.7% identical to KCP_HALAI, in contrast to the major KCPs with > 80% identity. The latter was about only 30% identical to Pinctada maxima aspein . With only 24% aspartic acid it contained much less than aspein (75%).
Broad sequence similarity comparisons of the major H. laevigata proteins to other biomineralising proteomes
Of the 80 H. laevigata proteins (collected in Additional file 28) included in our invertebrate-focused biomineralizing proteome comparison 46 (57.5%) returned some degree of sequence similarity below the arbitrary e-value threshold of 10e-6 (Fig. 6). With some exceptions we observed a general trend of phylogenetic proximity to H. laevigata yielding higher frequencies and higher levels of sequence similarity (Fig. 6). This was apparent with L. gigantea and H. asinina returning the highest overall frequencies of sequence similarity (33.3 and 26.6% respectively) although H. asinina is the more closely related to H. laevigata. H. asinina also possessed some of the most similar proteins to H. laevigata (primarily uncharacterised proteins) represented by the blue and green links in Fig. 6. Interestingly only 6.8% of the C. nemoralis (the only terrestrial pulmonate gastropod included in this analysis) biomineralising proteome shared any sequence similarity with that of H. laevigata. Also of note is the significant proportion of the C. gigas (a marine bivalve) shell-forming proteome shared with H. laevigata (24.5%). The proportions of all other bivalve proteomes that shared sequence similarity with H. laevigata ranged between 14.1 and 20.8%. The brachiopod M. venosa, the sea urchin S. purpuratus and the coral A. millepora shared the lowest proportions of similarity with H. laevigata (6.1, 6.5 and 13.5% respectively). Of the 46 H. laevigata proteins included in this comparison that shared some degree of similarity with another invertebrate biomineralising protein, 41 returned a significant match against proteins deposited in Swissprot (Fig. 6). Some of these (for example hemicentin) shared weak similarity with sequences in almost all species included in the analysis, while others (most noticeably the uncharacterized proteins 1, 2, 3, 5 and 6 and the ependymin-related proteins 1 and 2) were only found in the H. asinina dataset.
We also searched all 448 identified proteins against the complete UniProtKB/TrEMBL protein database. When we consider only the highest scoring matches of the FASTA search output (Additional file 4: Table S2, Additional file 5: Table S3), 78 Haliotis entries were returned (17% of the total). As discussed above, this number included almost all of the previously identified Haliotis shell proteins. The relatively small number of this group is also likely due to the low number of Haliotis proteins in the database. Another 21% (96 proteins) of the identified proteins were most similar to L. gigantea proteins, the sequences of which are derived from the L. gigantea genome sequencing project . However, only 28 of these 96 proteins were identified in the Lottia shell proteome (Additional file 4: Table S2, Additional file 5: Table S3). All of these were minor, or even trace, components of the shell matrix of both shells, with the exception of the major protein idb_4071, a short sequence stretch (aa162–270) of which did match to the major Lottia shell protein MRP_LOTGI (Additional file 4: Table S2) [56, 105]. The third large group of highest scoring matches was to Crassostrea gigas proteins (39 proteins, 9% of the total). However, only two of the oyster proteins were previously identified in the shell proteome of this bivalve. These were the minor proteins Tri_111928/K1QJ54_CRAGI and Comp52297_c0_seq1_2/K1R3V2 (Additional file 4: Table S2). Another 43 identified proteins were most similar in FASTA searches to various molluscs, the largest single fraction (22 minor proteins) originating from a combined transcriptomic and proteomic study of the shell-less terrestrial gastropod Arion vulgaris .
The shell matrix proteome presented in this study is the most comprehensive for a Haliotis species to date and with almost 450 identified proteins is also one of the most comprehensive published molluscan shell proteomes. It comprises almost all of the previously published Haliotis shell matrix proteins which, in most cases, were among the set of 77 major proteins (Table 1). A comparison of the proteomes of the nacreous and the prismatic shell layers indicated that most major proteins could be detected in both layers, but often with very different abundances (ie not always as major proteins). This was not the case in a comprehensive comparison of oyster nacreous and prismatic layers  and we interpret this difference to be due to the significant evolutionary distance between gastropods and bivalves. Furthermore, a previous comparison of oyster and abalone nacre forming transcriptomes also found surprisingly little in common , supporting the results reported here. It has been suggested that layer specific proteins may control the mineral polymorph and the crystal structure. However, the differences in mineral polymorph and microscopic structure of the two shell layers may depend not only on the presence or absence of certain proteins, but rather on their quantity.
Recent comparisons between mollusc shell proteomes [121, 126, 137, 138] and an increasing number of in-depth transcriptomic and proteomic studies are contributing to an ever-increasing list of novel proteins. The data that can support the concept of an ancestral “biomineralization toolkit” at least for the Mollusca increasingly appears to include a core group of enzymes such as carbonic anhydrases, peroxidases and tyrosinases, and proteins with repetitive low complexity domains and specifically biased amino acid composition. All of these features were also identified or predicted in many H. laevigata shell proteins (Table 1, Additional file 4: Table S2, Additional file 5: Table S3).
Unfortunately the determination of protein function is seriously lagging behind the rapid rate at which new shell matrix proteins are being identified. For many proteins the presence of a function, or at least an activity, is predicted by the presence of a conserved domain, as in the case of tyrosinase, carbonic anhydrase, chitin-binding and other domains. However, in very few cases experimental evidence for the respective activity has been obtained. Revealing the specific function of shell matrix proteins at the molecular level is clearly a major challenge for the coming years.
False discovery rate
Higher-energy collision-induced dissociation
Intensity-based absolute quantification
Intrinsically disordered protein
Intrinsically disordered region
Tandem mass spectrometry
Next generation sequencing
Polyacrylamide gel electrophoresis
Zaremba CM, Belcher AM, Fritz M, Li Y, Mann S, Hansma PK, Morse DE, Speck JS, Stucky GD. Critical transition in the biofabrication of abalone shells and flat pearls. Chem Mater. 1996;8:679–90.
Su X, Belcher AM, Zaremba CM, Morse DE, Stucky GD, Heuer AH. Structural and microstructural characterization of the growth lines and prismatic microarchitecture in red abalone shell and the microstructures of abalone ‘flat pearls‘. Chem Mater. 2002;14:3106–17.
Schäffer TE, Ionescu-Zanetti C, Proksch R, Fritz M, Walters DA, Almquist N, Zaremba CM, Belcher AM, Smith BL, Stucky GD, Morse DE, Hansma PK. Does abalone form by heteroepitaxial nucleation or by growth through mineral bridges? Chem Mater. 1997;9:1731–40.
Fritz M, Morse DE. The formation of highly organized biogenic polymer/ceramic composite materials: the high-performance microlaminate of molluscan nacre. Curr Opin Colloid Interface Sci. 1998;3:55–62.
Heinemann F, Launspach M, Gries K, Fritz M. Gastropod nacre: structure, properties and growth – biological, chemical and physical basis. Biophys Chem. 2011;153:126–53.
Jackson DJ, Reim L, Randow C, Cerveau N, Degnan BM, Fleck C. Variation in orthologous shell-forming proteins contributes to molluscan shell diversity. Mol Biol Evol. 2017;34:2959–69.
McDougall C, Green K, Jackson DJ, Degnan BM. Ultrastructure of the mantle of the gastropod Haliotis asinina and mechanism of shell regionalization. Cells Tissues Organs. 2011;194:103–7.
Belcher AM, Wu XH, Christensen RJ, Hansma PK, Stucky GD, Morse DE. Control of crystal phase switching and orientation by soluble mollusc-shell proteins. Nature. 1996;381:56–8.
Walters DA, Smith BL, Belcher AM, Paloczi GT, Stucky GD, Morse DE, Hansma PK. Modification of calcite crystal growth Ba abalone shell proteins: an atomic force microscope study. Biophys J. 1997;72:1425–33.
Thompson JB, Paloczi GT, Kindt JH, Michenfelder M, Smith BL, Stucky GD, Morse DW, Hansma PK. Direct observation of the transition from calcite to aragonite as induced by abalone shell proteins. Biophys J. 2000;79:3307–12.
Gries K, Heinemann F, Gummich M, Ziegler A, Rosenauer A, Fritz M. Influence of the insoluble and soluble matrix of abalone nacre on the growth of calcium carbonate crystals. Crystal Growth Design. 2011;11:729–34.
Smith BL, Schäffer TE, Viani M, Thompson JB, Frederick NA, Kindt J, Belcher A, Stucky GD, Morse DE, Hansma PK. Molecular mechanistic origin of the toughness of natural adhesives, fibres and composites. Nature. 1999;399:761–3.
Shen X, Belcher AM, Hansma PK, Stucky GD, Morse DE. Molecular cloning and characterization of lustrin a, a matrix protein from shell and pearl nacre of Haliotis rufescens. J Biol Chem. 1997;272(51):32472–81.
Mann K, Weiss IM, André S, Gabius HJ, Fritz M. The amino acid sequence of abalone (Haliotis laevigata) nacre protein perlucin. Detection of a functional C-type lectin domain with galactose/mannose specificity. Eur J Biochem. 2000;267:5257–64.
Blank S, Arnoldi M, Khoshnavaz S, Treccani L, Mann K, Grathwohl G, Fritz M. The nacre protein perlucin nucleates growth of calcium carbonate crystals. J Microsc. 2003;212:280–91.
Weiss IM, Göhring W, Fritz M, Mann K. Perlustrin, a Haliotis laevigata (abalone) nacre protein, is homologous to the insulin-like growth factor binding protein N-terminal module of vertebrates. Biochem Biophys Res Commun. 2001;285:244–9.
Michenfelder M, Fu G, Lawrence C, Weaver JC, Wustman BA, Taranto L, Evans JS, Morse DE. Characterization of two molluscan crystal-modulating biomineralization proteins and identification of putative mineral binding domains. Biopolymers. 2003;70:522–33.
Fu G, Valiyaveettil S, Wopenka B, Morse DE. CaCO3 biomineralization: acidic 8-kDa proteins from aragonitic abalone shell nacre can specifically modify calcite crystal morphology. Biomacromolecules. 2005;6:1289–98.
Treccani L, Mann K, Heinemann F, Fritz M. Perlwapin, an abalone nacre protein with three four-disulfide core (whey acidic protein) domains, inhibits the growth of calcium carbonate crystals. Biophys J. 2006;91:2601–8.
Mann K, Siedler F, Treccani L, Heinemann F, Fritz M. Perlinhibin, a cysteine-, histidine-, and arginine-rich miniprotein from abalone (Haliotis laevigata) nacre, inhibits calcium carbonate crystallization. Biophys J. 2007;93:1246–54.
Marie B, Marie A, Jackson DJ, Dubost L, Degnan B, Milet C, Marin F. Proteomic analysis of the organic matrix of the abalone Haliotis asinia calcified shell. Proteome Sci. 2010;8:54.
Bédouet L, Marie A, Berland S, Marie B, Auzoux-Bordenave S, Marin F, Milet C. Proteomic strategy for identifying mollusc shell proteins of insoluble organic shell matrix: a pilot study on Haliotis tuberculata. Mar Biotechnol. 2012;14:446–58.
Marie B, Joubert C, Tayalé A, Zanella-Cléon I, Belliard C, Piquemal D, Cochennec-Laureau N, Marin F, Gueguen Y, Montagnani C. Different secretory repertoires control the biomineralization processes of prism and nacre deposition of the pearl oyster shell. Proc Natl Acad Sci U S A. 2012;109:20986–91.
Liao Z, Bao L, Fan M, Gao P, Wang X, Qin C, Li X. In-depth proteomic analysis of nacre, prism, and myostracum of Mytilus shell. J Proteome. 2015;122:26–40.
Gao P, Liao Z, Wang X, Bao L, Fan M, Li X, Wu C, Xia S. Layer-by-layer proteomic analysis of Mytilus galloprovincialis shell. PLoS One. 2015;10:e0133913.
Weiss IM, Kaufmann S, Mann K, Fritz M. Purification and characterization of perlucin and perlustrin, two new proteins from the shell of the mollusc Haliotis laevigata. Biochem Biophys Res Commun. 2000;167:17–21.
Shevchenko A, Tomas H, Havlis J, Olsen JV, Mann M. In-gel digestion for mass spectrometric characterization of proteins and proteomes. Nat Protoc. 2006;1:2856–60.
Rappsilber J, Mann M, Ishihama Y. Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips. Nat Protoc. 2007;2:1896–906.
Wisniewski JR, Zougman A, Nagaraj N, Mann M. Universal sample preparation method for proteome analysis. Nat Methods. 2009;6:359–62.
Wisniewski JR, Zielinska DF, Mann M. Comparison of ultrafiltration units for proteomic and N-glycoproteomic analysis by the filter-aided sample preparation method. Anal Biochem. 2011;410:307–9.
Olsen JV, Schwartz JC, Griep-Raming J, Nielsen ML, Damoc E, Denisov E, Lange O, Remes P, Taylor D, Splendore M, Wouters ER, Senko M, Makarov A, Mann M, Horning S. A dual pressure linear ion trap-Orbitrap instrument with very high sequencing speed. Mol Cell Proteomics. 2009;8:2759–69.
Michalski A, Damoc E, Lange O, Denisov E, Nolting D, Müller M, Viner R, Schwartz J, Remes P, Belford M, Dunyach JJ, Cox J, Horning S, Mann M, Makarov A. Ultrahigh resolution linear ion trap orbitrap mass spectrometer (Orbitrap elite) facilitates top down LC MS/MS and versatile peptide fragmentation modes. Mol Cell Proteomics. 2012;11 https://doi.org/10.1074/mcp.O111.013698.
Cox J, Mann M. MaxQuant enables high peptide identification rates, individualized ppb-range mass accuracies and proteome-wide protein quantification. Nature Biotechnol. 2009;26:1367–72.
Cox J, Matic I, Hilger M, Nagaraj N, Selbach M, Olsen JV, Mann M. A practical guide to the MaxQuant computational platform for SILAC-based quantitative proteomics. Nat Protoc. 2009;4:698–705.
Tynova S, Temu T, Carlson A, Sinitcyn P, Mann M, Cox J. Visualization of LC-MS/MS proteomics data in MaxQuant. Proteomics. 2015;15:1453–6.
Tynova S, Temu T, Cox J. The MaxQuant computational platform for mass spectrometry-based shotgun proteomics. Nat Protoc. 2016;12:2301–19.
Cox J, Neuhauser N, Michalski A, Scheltema RA, Olsen JV, Mann M. Andromeda – a peptide search engine integrated into the MaxQuant environment. J Proteome Res. 2011;10:1794–805.
Shiel BP, Hall NE, Cooke IR, Robinson NA, Strugnell JM. De novo characterization of the greenlip abalone transcriptome (Haliotis laevigata) with focus on the heat shock protein 70 (HSP70) family. Mar Biotechnol. 2015;17:23–32.
Li W, Cowley A, Uludaq M, Gur T, McWilliams H, Squizzato S, Park YM, Buso N, Lopez R. The EMBL-EBI bioinformatics web and programmatic tools framework. Nucleic Acids Res. 2015;43(Web Server issue):W580–4.
Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 2014;30:2114–20.
Cerveau N, Jackson DJ. Combining independent de novo assemblies optimizes the coding transcriptome for nonconventional model eukaryotic organisms. BMC Bioinformatics. 2016;17:525.
Haas BJ, Papanicolaou A, Yassour M, Grabherr M, Blood PD, Bowden J, Couger MB, Eccles D, Li B, Lieber M, MacManes MD, Ott M, Orvis J, Pochet N, Strozzi F, Weeks N, Westerman R, William T, Dewey CN, Henschel R, LeDuc RD, Friedman N, Regev A. De novo transcript sequence reconstruction from RNA-seq using the trinity platform for reference generation and analysis. Nat Protocols. 2013;8:1494–512.
Peng Y, Leung HCM, Yiu S-M, Lv M-J, Zhu X-G, Chin FYL. IDBA-Tran: a more robust de novo de Bruijn graph assembler for transcriptomes with uneven expression levels. Bioinformatics. 2013;29:i326–34.
Neuhauser N, Michalski A, Cox J, Mann M. Expert system for computer-assisted annotation of MS/MS spectra. Mol Cell Proteomics. 2012;11:1500–9.
Vizcaíno JA, Csordas A, del-Toro N, Dianes JA, Griss J, Lavidas I, Mayer G, Perez-Riverol Y, Reisinger F, Ternent T, Xu QW, Wang R, Hermjakob H. 2016 update of the PRIDE database and related tools. Nucleic Acids Res. 2016;44(D1):D447–56.
Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997;25:3389–402.
Finn RD, Attwood TK, Babbitt PC, Bateman A, Bork P, Bridge AJ, Chang H, Dosztányi Z, El-Gebali S, Fraser M, Gough J, Haft D, Holliday GL, Huang H, Huang X, Letunic I, Lopez R, Lu S, Marchler-Bauer A, Mi H, Mistry J, Natale DA, Necci M, Nuka G, Orengo CA, Park Y, Pesseat S, Piovesan D, Potter SC, Rawlings ND, Redaschi N, Richardson L, Rivoire C, Sangrador-Vegas A, Sigrist C, Sillitoe I, Smithers B, Squizzato S, Sutton G, Thanki N, Thomas PD, Tosatto SCE, Wu CH, Xenarios I, Yeh L, Young S, Mitchell AL. InterPro in 2017 — beyond protein family and domain annotations. Nucleic Acids Res. 2017;45(Database issue):D190–9.
Petersen TN, Brunak S, von Heinje G, Nielsen H. SignalP 4.0: discriminating signal peptides from transmembrane regions. Nat Methods. 2011;8:785–6.
Mizianty MJ, Stach W, Chen K, Kedarisetti KD, Disfani FM, Kurgan L. Improved sequence-based prediction of disordered regions with multilayer fusion of multiple information sources. Bioinformatics. 2010;26:i489–96.
Mizianty MJ, Zhang T, Xue B, Zhou Y, Dunker AK, Uversky VN, Kurgan LA. In-silico prediction of disorder content using hybrid sequence representation. BMC Bioinformatics. 2011;12(1):245.
Mizianty MJ, Peng Z, Kurgan LA. MFDp2 - accurate predictor of disorder in proteins by fusion of disorder probabilities, content and profiles. Intrinsically Disordered Proteins. 2013;1(1):e24428.
Gasteiger E, Hoogland C, Gattiker A, Duvaud S, Wilkins MR, Appel RD, Bairoch A. Protein Identification and analysis tools on the ExPASy server. In: Walker JM, editor. The proteomics protocols handbook, Humana press; 2005. p. 571–607.
Newman AM, Cooper BC. XSTREAM: a practical algorithm for identification and architecture modeling of tandem repeats in protein sequences. BMC Bioinformatics. 2007;8:382.
Ishida T, Kinoshita K. PrDOS: prediction of disordered protein regions from amino acid sequence. Nucleic Acids Res. 2007;35:W460–4.
Dosztányi Z, Csizmók V, Tompa P, Simon I. The pairwise energy content estimated from amino acid composition discriminates between folded and intrinsically unstructured proteins. J Mol Biol. 2005;347:827–39.
Mann K, Jackson DJ. Characterization of the pigmented shell-forming proteome of the common grove snail Cepaea nemoralis. BMC Genomics. 2014;15:249.
Jackson DJ, McDougall C, Green K, Simpson F, Wörheide G. Degnan BM. A rapidly evolving secetome builds and patterns a sea shell. BMC Biol. 2006;4:40.
Mann K, Edsinger E. The Lottia gigantea shell matrix proteome: re-analysis including MaxQuant iBAQ quantitation and phosphoproteome analysis. Proteome Sci. 2014;12:28.
Feng D, Li Q, Yu H, Kong L, Du S. Identification of conserved proteins from diverse shell matrix proteome in Crassostrea gigas: characterization of genetic bases regulating shell formation. Sci Rep. 2017;7:45754.
Arivalagan J, Marie B, Sleight VA, Clark MS, Berland S, Marie A. Shell matrix proteins of the clam, Mya truncata: roles beyond shell formation through proteomic study. Mar Genomics. 2016;27:69–74.
Liu C, Li S, Kong J, Liu Y, Wang T, Xie L, Zhang R. In-depth proteomic analysis of shell matrix proteins of Pinctada fucata. Sci Rep. 2015;5:17269.
Jackson DJ, Mann K, Häussermann V, Schilhabel MB, Lüter C, Griesshaber E, Schmahl W, Wörheide G. The Magellania venosa biomineralizing proteome: a window into brachiopod shell evolution. Genome Biol Evol. 2015;7:1349–62.
Mann K, Poustka AJ, Mann M. In-depth, high-accuracy proteomics of sea urchin tooth organic matrix. Proteome Sci. 2008;6:33.
Ramos-Silva P, Kaandorp J, Herbst F, Plasseraud L, Alcaraz G, Stern C, Corneillat M, Guichard N, Durlet C, Luquet G, Marin F. The skeleton of the staghorn coral Acropora millepora: molecular and structural characterization. PLoS One. 2014;9:e97454.
Smith SA, Wilson NG, Goetz FE, Feehery C, Andrade SCS, Rouse GW, Giribet G, Dunn CW. Resolving the evolutionary relationships of molluscs with phylogenomic tools. Nature. 2011;480:364–7.
González VL, Andrade SCS, Bieler R, Collins TM, Dunn CW, Mikkelsen PM, Taylor JD, Giribet G. A phylogenetic backbone for Bivalvia: an RNA-seq approach. Proc R Soc B: Biological Sciences. 2015;182:2014–332.
Simion P, Philippe H, Baurain D, Jager M, Richter DJ, Di Franco A, Roure B, Satoh N, Quéinnec E, Ereskovsky A, Lapébie P, Corre E, Delsuc F, King N, Wörheide G, Manuel M. A large and consistent phylogenomic dataset supports sponges as sister group to all other animals. Curr Biol. 2017;27:958–67.
Paps J, Baguñà J, Riutort M. Lophotrochozoa internal phylogeny: new insights from an up-to-date analysis of nuclear ribosomal genes. Proc R Soc B Biological Sciences. 2009;276:1245–54.
Mann K, Edsinger-Gonzales E, Mann M. In-depth proteomic analysis of a mollusc shell: acid-soluble and acid-insoluble matrix of the limpet Lottia gigantea. Proteome Sci. 2012;10:28.
Gotliv BA, Addadi L, Weiner S. Mollusk shell acidic proteins: in search of individual functions. ChemBioChem. 2003;4:522–9.
Dodenhof T, Dietz F, Franken S, Grunwald I, Kelm S. Splice variants of perlucin from Haliotis laevigata modulate the crystallisation of CaCO3. PLoS One. 2014;9:e97126.
Rami Al Shweiki MHD, Mönchgesang S, Majovski P, Thieme D, Trutschel D, Hoehenwarter W. Assessment of label-free quantification in discovery proteomics and impact of technological factors and natural variability of protein abundance. J Proteome Res. 2017;16:1410–24.
Sudakov NP, Klimenkov IV, Byvaltsev VA, Nikiforov SB, Konstantinov YM. Extracellular actin in health and disease. Biochem Mosc. 2017;82:1–12.
Weiss IM, Schönitzer V, Eichner N, Sumper M. The chitin synthase involved in marine bivalve mollusk shell formation contains a myosin domain. FEBS Lett. 2006;580:1846–52.
Weiss IM. Species-specific shells: chitin synthases and cell mechanics in molluscs. Z Kristallogr. 2012;227:723–38.
Sarashina I, Endo K. Primary structure of a soluble matrix protein of scallop shell: implications for calcium carbonate biomineralization. Am Mineral. 1998;83:1510–5.
Sarashina I, Endo K. The complete primary structure of molluscan shell protein 1 (MSP-1), an acidic glycoprotein in the shell matrix of the scallop Patinopecten yessoensis. Mar Biotechnol. 2001;3:362–9.
Suzuki M, Murayama E, Inoue H, Ozaki N, Tohse H, Kogure T, Nagasawa H. Characterization of Prismalin-14, a novel matrix protein from the prismatic layer of the Japanese pearl oyster (Pinctada fucata). Biochem J. 2004;382:205–13.
Tsukamoto D, Sarashina I, Endo K. Structure and expression of an unusually acid matrix protein of pearl oyster shells. Biochem Biophys Res Commun. 2004;320:1175–80.
Weiner S, Addadi L. Acidic macromolecules of mineralized tissues: the controllers of crystal formation. Trends Biochem Sci. 1991;16:252–6.
Marin F, Luquet G. Unusually acidic proteins in biomineralization. In: Bäuerlein E, editor. Handbook of Biomineralization. Weinheim: Wiley-VCH; 2007. p. 273–90.
Marin F, Luquet G, Marie B, Medakovic D. Molluscan shell proteins: primary structure, origin, and evolution. Curr Topics Dev Biol. 2008;80:209–75.
McDougall C, Woodcroft BJ, Degnan BM. The widespread prevalence and functional significance of silk-like structural proteins in metazoan biological materials. PLoS One. 2016;11:e0159128.
Sudo S, Fujikawa T, Nagakura T, Ohkubo T, Sakaguchi K, Tanaka M, Nakashima K, Takahashi T. Structures of mollusc shell framework proteins. Nature. 1997;387:563–4.
Miyamoto H, Yano M, Miyashita T. Similarities in the structure of nacrein, the shell-matrix protein, in a bivalve and a gastropod. J Molluscan Stud. 2003;69:87–9.
Montagnani C, Marie B, Marin F, Belliard C, Riquet F, Tayalé A, Zanella-Cléon I, Fleury E, Gueguen Y, Piquemal D, Cochennec-Laureau N. Pmarg-Pearlin is a matrix protein involved in nacre framework formation in the pearl oyster Pinctada margaritifera. Chembiochem. 2011;12:2033–43.
Tompa P. Unstructural biology coming of age. Curr Opin Struct Biol. 2011;21:419–25.
Uversky VN. Intrinsically disordered proteins from a to z. Int J Biochem Cell Biol. 2011;43:1090–103.
Peng Z, Yan J, Fan X, Mizianty MJ, Xue B, Wang k HG, Uversky VN, Kurgan L. Exceptionally abundant exceptions: comprehensive characterization of intrinsic disorder in all domains of life. Cell Mol Life Sci. 2015;72:137–51.
Kalmar L, Homola D, Varga G, Tompa P. Structural disorder in proteins brings order to crystal growth in biomineralization. Bone. 2012;51:528–34.
Boskey AL, Villarreal-Ramirez E. Intrinsically disordered proteins and biomineralization. Matrix Biol. 2016;52-54:43–59.
Wojtas M, Dobroszycki P, Ozyhar A. Intrinsically disordered proteins in biomineralization. In: Seto J, editor. Advanced topics in biomineralization. InTechOpen; 2012. p. 3–32. https://doi.org/10.5772/1095.
Weber E, Weiss IM, Cölfen H, Kellermeier M. Recombinant perlucin derivatives influence the nucleation of calcium carbonate. Cryst Eng Comm. 2016;18:8439–44.
Mount AS, Wheeler AP, Paradkar RP, Snider D. Hemocyte-mediated shell mineralization in the eastern oyster. Science. 2004;304:297–300.
Li S, Liu Y, Liu C, Huang J, Zheng G, Xie L, Zhang R. Hemocytes participate in calciumcarbonate crystal formation, transportation and shell regeneration in the pearl oyster Pinctada fucata. Fish Shellfish Immunol. 2016;51:263–70.
Gaume B, Denis F, Van Wormhoudt A, Huchette S, Jackson DJ, Avignon S, Auzozx-Bordenave S. Characterization and expressin of the biomineralising gene lustrin a during shell formation of the European abalone Haliotis tuberculata. Comp Biochem Physiol B. 2014;169:1–8.
Kim IW, Morse DE, Evans JS. Molecular characterization of the 30-aa N-terminal mineral interaction domain of the biomineralization protein AP7. Langmuir. 2004;20:11664–73.
Collino S, Kim IW, Evans JS. Identification and structural characterization of an unusual RING-like sequence within an extracellular biomineralization protein AP7. Biochemistry. 2008;47:3745–55.
Amos FF, Ndao M, Ponce CB, Evans JP. A C-RING-like domain participates in protein self-assembly and mineral nucleation. Biochemistry. 2011;50:8880–7.
Perovic I, Verch A, Chang EP, Rao A, Cölfen H, Kröger R, Evans JS. An oligomeric C-ring nacre protein influences prenucleation events and organizes mineral nanoparticles. Biochemistry. 2014;53:7259–68.
Amos FF, Evans JS. AP7, a partially disordered pseudo C-ring protein, is capable of forming stabilized aragonite in vitro. Biochemistry. 2009;48:1332–9.
Collino S, Evans JS. Structural features that distinguish kinetically distinct biomineralization polypeptides. Biomacromolecules. 2007;8:1686–94.
Tanasawet S, Withyachumnarnkul B, Changsangfar C, Cummins SF, Sroyraya P, Kitiyanant Y, Asuvapongpatana S, Weerachatyanukul. Isolation of organic matrix nacreous proteins from Haliotis diversicolor and their effect on in vitro osteoinduction. Malacologia. 2013;56:107–19.
Le Roy N, Jackson DJ, Marie B, Ramos-Silva P, Marin F. The evolution of metazoan a-carbonic anhydrases and their roles in calcium carbonate biomineralization. Front Zool. 2014;11:75.
Marie B, Jackson DJ, Ramos-Silva P, Zanella_Cleon I, Guichard N, Marin F. The shell-forming proteome of Lottia gigantea reveals both deep conservation and lineage-specific novelties. FEBS J. 2013;280:214–32.
Le Roy N, Marie B, Gaume B, Guichard N, Delgado S, Zanella-Cléon I, Becchi M, Auzoux-Bordenave S, Sire J-Y, Marin F. Identification of two carbonic anhydrases in the mantle of the European abalone Haliotis tuberculata (Gastropoda, Haliotidae): phylogenetic implications. J Exp Zool (Mol Dev Evol). 2012;318B:353–67.
Werner GDA, Gemmel P, Grosser S, Hamer R, Shimeld SM. Analysis of a deep transcriptome from the mantle tissue of Patella vulgata Linnaeus (Mollusca: Gastropoda: Patellidae) reveals candidate biomineralising genes. Mar Biotechnol. 2013;15:230–43.
Zhang C, Xie L, Huang J, Chen L. Zhang R. A novel putative tyrosinase involved in periostracum formation from the pearl oyster (Pinctada fucata). Biochem Biophys Res Commun. 2006;342:632–9.
Nagai K, Yano M, Morimoto K, Miyamoto H. Tyrosinase localization in mollusc shells. Comp Biochem Physiol B. 2007;146:207–14.
Aguilera F, McDougall C, Degnan BM. Evolution of the tyrosinase gene family in bivalve molluscs: independent expansion of the mantle gene repertoire. Acta Biomineral. 2014;10:3855–65.
Chen X, Liu X, Bai Z, Zhao L, Li J. HcTyr and HcTyp-1 of Hyriopsis cumingii, novel tyrosinase and tyrosinase-related protein genes involved in nacre color formation. Comp Biochem Biophys B. 2017;204:1–8.
Timmermans LPM. Studies on shell formation in molluscs. Netherlands J Zool. 1969;19:417–523.
Hüning AK, Lange SM, Ramesh K, Jacob D, Jackson DJ, Panknin U, Gutowska MA, Philipp EER, Rosenstiel P, Lucassen M, Melzner F. A shell regeneration assay to identify biomineralization candidate genes in mytilid mussels. Mar Genomics. 2016;27:57–67.
Weiner S, Traub W. X-ray diffraction study of the insoluble organic matrix of mollusk shells. FEBS Lett. 1980;111:311–6.
Suzuki M, Saruwatari K, Kogure T, Yamamoto Y, Nishimura T, Kato T, Nagasawa H. An acidic matrix protein, Pif, is a key macromolecule for nacre formation. Science. 2009;325:1388–90.
Suzuki M, Iwashima A, Tsutsui N, Ohira T, Kogure T, Nagasawa H. Identification and characterization of a calcium carbonate-binding protein, blue mussel shell protein (BMSP), from the nacreous layer. Chembiochem. 2011;12:2478–87.
Suzuki M, Iwashima I, Kimura M, Kogure T, Nasagawa H. The molecular evolution of the Pif family proteins in various species of molluscs. Mar Biotechnol. 2013;15:145–58.
Marin F, Luquet G. Molluscan shell proteins. C R Palevol. 2004;3:469–92.
Marin F, Le Roy N, Marie B. The formation and mineralization of mollusc shell. Front Biosci. 2012;S4:1099–125.
McDougall C, Aguilera F, Degnan BM. Rapid evolution of pearl oyster shell matrix proteins with repetitive, low-complexity domains. J R Soc Interface. 2017;10:20130041.
Jackson DJ, McDougall C, Woodcroft B, Moase P, Rose RA, Kube M, Reinhardt R, Rokhsar DS, Montagnani C, Joubert C, Piquemal D, Degnan BM. Parallel evolution of nacre building gene sets in molluscs. Mol Biol Evol. 2010;27:591–608.
Isowa Y, Sarashina I, Setiamarga DHE, Endo K. A comparative study of the shell matrix protein aspein in pterioid bivalves. J Mol Evol. 2012;75:11–8.
Gotliv B, Kessler N, Sumerel JL, Morse DE, Tuross N, Addadi L, Weiner S. Asprich: a novel aspartic acid-rich protein family from the prismatic shell matrix of the bivalve Atrina rigida. Chembiochem. 2005;6:304–14.
Kono M, Hayashi N, Samata T. Molecular mechanism of the nacreous layer formation in Pinctada maxima. Biochem Biophys Res Commun. 2000;269:313–218.
Sarashina I, Endo K. Skeletal matrix proteins of invertebrate animals: comparative analysis of their amino acid sequences. Paleont Res. 2006;10:311–36.
Aguilera F, McDougall C, Degnan BM. Co-option and de novo gene evolution underlie molluscan shell diversity. Mol Biol Evol. 2017;34:779–92.
Kocot KM, Aguilera F, McDougall C, Jackson DJ, Degnan BM. Sea shell diversity and rapidly evolving secretomes: insights into the evolution of biomineralisation. Frontiers Zool. 2016;13:23.
Waite JH. Evidence for the mode of sclerotization in a molluscan periostracum. Comp Biochem Physiol. 1977;58B:157–62.
Marxen JC, Witten PE, Fincke D, Reelsen O, Rezgaoui M. Becker W. A light- and electron microscopic study of enzymes in the embryonic shell-forming tissue of the freshwater snail, Biophalaria glabrata. Invertebrate. Biol. 2003;122:313–25.
Hohagen J, Jackson DJ. An ancient process in a modern mollusc: early development of the shell in Lymnea stagnalis. BMC Dev Biol. 2013;13:27.
Mann K, Wilt FH, Poustka AJ. Proteomic analysis of sea urchin (Strongylocentrotus purpuratus) spicule matrix. Proteome Sci. 2010;8:33.
Simakov O, Marletaz F, Cho SJ, Edsinger-Gonzales E, Havlak P, Hellsten U, Kuo DH, Larsson T, Lv J, Arendt D, Savage R, Osoegawa K, de Jong P, Grimwood J, Chapman JA, Shapiro H, Aerts A, DS ORPR. Insights into bilaterian evolution from three spiralian genomes. Nature. 2013;493:526–31.
Zhang G, Fang X, Guo X, Li L, Luo R, Xu F, Yang P, Zhang L, Wang X, Qi H, Xiong Z, Que H, Xie Y, Holland PWH, Paps J, Zhu Y, Wu F, Chen Y, Wang J. The oyster genome reveals stress adaptation and complexity of shell formation. Nature. 2012;490:49–54.
Wang GL, Xu B, Bai ZY, Li JJ. Two chitin metabolic enzyme genes from Hyriopsis cumingii: cloning, characterization, and potential functions. Genet Mol Res. 2012;11:4539–51.
Marie B, Le Roy N, Zanella-Cleon I, Becchi M, Marin F. Molecular evolution of mollusc shell proteins: insights from proteomic analysis of the edible mussel Mytilus. J Mol Evol. 2011;72:531–46.
Bulat T, Smidak R, Sialana F, Jung G, Rattei T, Bilban M, Sattmann H, Lubec G, Aradska J. Transcriptomic and proteomic analysis of Arion vulgaris – proteins for probably successful survival strategies? PLoS One. 2016;11:e0150614.
Jackson DJ, Degnan BM. The importance of evo-devo to an integrated understanding of molluscan biomineralisation. J Struct Biol. 2016;196:67–4.
Arivalagan J, Yarra T, Marie B, Sleight VA, Duvernois-Berthet E, Clark MS, Marie A, Berland S. Insights from shell proteome: biomineralization to adaptation. Mol Biol Evol. 2017;34:66–77.
The authors acknowledge Gaby Sowa (MPI) for preparing the capillary columns, Korbinian Mayr and Igor Paron (both MPI) for keeping the mass spectrometers in excellent condition, and Mario Oroshi (MPI) for his help with data submission to the PRIDE repository. Gabriela Salinas-Riester and her team at the Göttingen TAL sequencing centre performed the NGS. We also thank Joel Gilby (Ocean Wave Seafoods) for providing access to Ocean Wave Seafood abalone stock, and his assistance with collecting abalone mantle tissue for RNA extractions.
This research did not receive any specific grant from funding agencies in the public, commercial, or other sectors.
Availability of data and materials
Sequences from mantle transcriptomics are available from GenBank under SRP126753. The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PXD009567.All other data generated are included in this published article including Additional files.
Ethics approval and consent to participate
The authors declare that they have no competing interests.
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Confirmed reading frames of the hemolymph and tentacle H. laevigata database. This docx-file contains a compilation of all reading frames translated from the nucleic acid sequence database of  confirmed by MS/MS-derived peptide sequences. Only majority proteins (shortest sequence containing most peptides) of MaxQuant ProteinGroups output tables are shown. Identifications not accepted, for instance most single-peptide identifications, are also included. Identified peptides are in blue. (DOCX 697 kb)
Table S1. Organic matrix yields. This docx-file shows the organic matrix yields of individual shell fractions as determined by weighing after lyophilisation of acidic extracts. (DOCX 14 kb)
Figure S1. SDS-PAGE of shell organic matrix. This figure in jpg format shows a SDS-PAGE comparison between the nacre acid-soluble fraction obtained with different protocols A, B and C, and comparison of prismatic layer acid-insoluble fractions A and B. Similar amounts of matrix (ca. 200 μg) were applied to each lane. (JPG 1284 kb)
Table S2. Nacre proteins. docx-file listing all accepted identifications of Haliotis laevigata nacre proteins including most similar database matches, number of identified peptides and abundance in different shell fractions. (DOCX 306 kb)
Table S3. Prismatic layer proteins. docx-file listing all accepted identifications of Haliotis laevigata prismatic layer proteins including most similar database matches, number of identified peptides and abundance in different shell fractions. (DOCX 309 kb)
ProteinGroups, nacre acid-insoluble, protocol A. Slightly modified MaxQuant output table in xlsx format showing identified protein groups/proteins including those not finally accepted for various reasons. The table contains all accession numbers and various parameters such as iBAQ intensity, peptide count, sequence coverage, protein score and molecular weight. Contaminant and reversed sequence hits were removed. Identified vertebrate contaminating proteins were removed. (XLSX 103 kb)
ProteinGroups, nacre acid-soluble, protocol A. See legend to Additional file 6. (XLSX 167 kb)
ProteinGroups, nacre acid-insoluble, protocol B. See legend to Additional file 6. (XLSX 141 kb)
ProteinGroups, nacre acid-soluble, protocol B. See legend to Additional file 6. (XLSX 174 kb)
ProteinGroups, nacre acid-insoluble, protocol C. See legend to Additional file 6. (XLSX 179 kb)
ProteinGroups, nacre acid-soluble, protocol C. See legend to Additional file 6. (XLSX 112 kb)
ProteinGroups, prismatic layer acid-insoluble, protocol A. See legend to Additional file 6. (XLSX 245 kb)
ProteinGroups, prismatic layer acid-soluble, protocol A. See legend to Additional file 6. (XLSX 58 kb)
ProteinGroups, prismatic layer acid-insoluble, protocol B. See legend to Additional file 6. (XLSX 271 kb)
ProteinGroups, prismatic layer acid-soluble, protocol B. See legend to Additional file 6. (XLSX 53 kb)
Distribution of nacre and prismatic layer proteins showing a summary of the distribution of the peptides of each identified protein among gel slices (fraction 1 to fraction 12). Fraction 111 shows the number of peptides in in-solution (FASP)-digested samples. Nacre proteins are contained in lines 3 to 641, prismatic layer proteins in lines 646 to 1285. The peptide distribution was derived from MaxQuant output files obtained by analysis of combined nacre sample raw-files and combined prismatic layer raw-files. (XLSX 303 kb)
Peptides, nacre acid-insoluble, protocol A. Slightly modified MaxQuant output table in xlsx format showing peptides to corresponding ProteinGroups files. The table contains the peptide sequences and various parameters such as peptide length, peptide mass, number of missed cleavages, charges, posterior error probabilities (PEP), peptide scores and peak intensities. Contaminant and reversed sequence hits were removed. (XLSX 287 kb)
Peptides, nacre acid-soluble, protocol A. See legend to Additional file 17. (XLSX 432 kb)
Peptides, nacre acid-insoluble, protocol B. See legend to Additional file 17. (XLSX 547 kb)
Peptides, nacre acid-soluble, protocol B. See legend to Additional file 17. (XLSX 587 kb)
Peptides, nacre acid-insoluble, protocol C. See legend to Additional file 17. (XLSX 555 kb)
Peptides, nacre acid-soluble, protocol C. See legend to Additional file 17. (XLSX 339 kb)
Peptides, prismatic layer acid-insoluble, protocol A. See legend to Additional file 17. (XLSX 902 kb)
Peptides, prismatic layer acid-soluble, protocol A. See legend to Additional file 17. (XLSX 884 kb)
Peptides, prismatic layer acid-insoluble, protocol B. See legend to Additional file 17. (XLSX 134 kb)
Peptides, prismatic layer acid-soluble, protocol B. See legend to Additional file 17. (XLSX 116 kb)
Figure S2. Sequences and repeat structure of uncharacterized major proteins. Sequence regions covered by identified peptides are shown in bold green. Predicted signal sequence peptides are underlined. Collagen triple-helical sequences are in italics. In sequence alignments identical amino acids are shaded yellow. (DOCX 75 kb)
Sequences of proteins used in proteome comparison. Conceptually derived protein sequences of 80 H. laevigata shell-forming proteins used in the generation of the Circoletto figure (Fig. 6). These sequences represent the 77 most abundant sequences from the shell described in Table 1 (77 proteins), and the minor proteins UP6 and UP7 (reported by Marie et al. ) which are encoded by three contigs. (TXT 32 kb)
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Mann, K., Cerveau, N., Gummich, M. et al. In-depth proteomic analyses of Haliotis laevigata (greenlip abalone) nacre and prismatic organic shell matrix. Proteome Sci 16, 11 (2018). https://doi.org/10.1186/s12953-018-0139-3
- Mantle transcriptome
- Shell organic matrix
- Prismatic layer