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. Author manuscript; available in PMC: 2009 Aug 25.
Published in final edited form as: Biochemistry. 2009 Jun 16;48(23):5254–5262. doi: 10.1021/bi9002953

Table 1. Identification of CgA and ProSAAS Protein Forms by N-Terminal Peptide Sequencing.

Protein spots from 2-D gel separation of the soluble fraction of purified chromaffin granules were transferred to PVDF membranes, and membrane regions corresponding to designated protein spots were excised for N-terminal peptide sequencing by Edman degradation. The determined N-terminal amino acid sequences for each protein spot is indicated. If more than one protein sequence was identified, their deduced primary sequences are indicated. The properties of each protein spot are illustrated for apparent molecular weight (on 2-D gels), apparent isoelectric point (pI), identification of the N-terminal sequences as CgA (or ProSAAS for spot #37), and relative protein staining by amido black on PVDF membranes of the 2-D gel proteins.

Spot #s N-terminal Sequences by
Edman Degradation
Ratios Apparent MW
range (kD)
Apparent pI CgA/ Fragment ID Relative Protein
Staining
1 LPVNSPMNKG 153 4.65 CgA Low
2,3 LPVNSPMNKG 66 4.55 – 4.62 CgA Very High
4 1°: HSSYEDELSE
2°: LPVNSPMNK
4 to 1 59 4.39 CgA Medium
5 1°: HSSYEDELSE
2°: LPVNSPMNKG
1 to 1 56 4.39 CgA Low
6 1°: DDFKEVEKSD
2°: LPVNSPMNKG
3 to 1 50 4.39 CgA Medium to Low
7 LPVNSPMNKG 45 4.39 CgA Medium to Low
8,9,10,11 AAPGWPEDGA 27 – 28 4.68 – 4.79 CgA Medium
12 LPVNSPMNKG 16 4.81 CgA Medium to Low
13 LPVNSPMNKG 15.5 4.95 CgA Medium to Low
14,15,16,17 LEGEEEEEED 14.5 – 15 4.60 – 4.81 CgA Medium
18 GWRPNNNRED Below 14.4 4.47 CgA Medium to Low
36 1°: ERGEVG_EER
2°: LPVNSPMNKG
ND 24 4.88 CgB &
CgA
Low
37 1°: LPVNSPMNKG
2°: AAPRGEAAGA
1 to 1 18 4.79 CgA &
ProSAAS (PC1
inhibitor)
Low Low