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Table 1 Table 1 Summary of the mass spectrometry analysis

From: Identification and structural analysis of C-terminally truncated collapsin response mediator protein-2 in a murine model of prion diseases

 

2-DEb)

Mass spectrometry

Theoreticalb)

Fold changed)(160dai)

p e)

Spot a)

Mr obs (kDa)

pI obs

Method

Identity

UniProt KB accession

Coverage

Number of peptides

Mowse score c)

Mr cal (kDa)

pI cal

  

a

56

5.45

MALDI & LC-ESI

CRMP-2-ΔC

O08553

39

17

963

56.5f)

5.48f)

7.96

0.076

b1

61

5.77

MALDI & LC-ESI

CRMP-2

O08553

45

22

1419

62.3g)

5.95g)

0.53

0.375

b2

61

5.72

MALDI & LC-ESI

CRMP-2

O08553

8

4

61

62.3

5.95h)

0.39

0.249

b3

61

5.68

MALDI & LC-ESI

CRMP-2

O08553

7

4

103

62.3

5.95h)

0.51

0.350

1

43

5.1

MALDI

GFAP

P03995

39

13

79

49.9

5.28

0.85

0.823

2

41

5.02

MALDI

GFAP

P03995

48

18

155

49.9

5.28

1.33

0.628

3

40

4.85

MALDI

GFAP

P03995

25

9

66

49.9

5.28

8.93

0.056

4

27

7.4

LC-ESI

Glutathione S- transferase μ1

P10649

21

7

176

25.8

8.14

+++ i)

ND

5

26

5.79

MALDI

Peroxiredoxin -6

O08709

44

8

121

24.7

5.72

1.58

0.389

6

24

5.02

LC-ESI

Peroxiredoxin -2

Q61171

38

8

372

21.6

5.2

0.90

0.850

  1. a) The spots shown in Figure 1.
  2. b) Mrobs and Mrcal, observed and theoretical Mr; pIobs and pIcal, observed and theoretical pI, respectively.
  3. c) Probability-based Mowse score [52] calculated using MASCOT software [48].
  4. d) Fold change of spot volume on 160 dai.
  5. e) p-Value of Student's t-test. ND: not determined.
  6. f) Mrcal and pIcal of non-phosphorylated CRMP-21-517.
  7. g) Mrcal and pIcal of non-phosphorylated CRMP-21-572.
  8. h) An approximate shift of -0.05 per phosphate moiety is expected [25, 26].
  9. i) Undetectable in the mock sample.