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. 2016 Jun 27;7(10):6440–6449. doi: 10.1039/c6sc02032a

Table 1. Fragment ions from various peptides upon dissociation within the SCGD. Only fragments with m/z ≥ 150 are included. Sequence coverage of the SCGD, compared to ESI-MS with CID, is also shown.

Name, # residues Peptide sequence an bn cn xn yn dn Internal fragments Identified residues
SCGD ESI-MS/MS
Renin substrate I, 8 Suc-RPFHLLVY-AMC 2–8 1–8 a5, a7 8/8, 100% 4/8, 50%
Angiotensin I, 10 DRVYIHPFHL 4, 7–10 5, 8 2–10 a6, b6 10/10, 100% 3/10, 30%
Angiotensin II, 8 DRVYIHPF 6 5–8 4 3–8 8/8, 100% 2/8, 25%
Bradykinin, 9 RPPGFSPFR 5 5, 7–9 4, 5 2–9 a6, a9 9/9, 100% 3/9, 33%
Substance P, 11 RPKPQQFFGLM 5, 7, 8, 10 3–11 4–10 8–11 a6, a11 11/11, 100% 6/11, 55%
SAMS peptide, 15 Biotin-HMRSAMpSGLHLVKRR 1, 2 1–3 1–6 GLHLV+, [SGLHLVKR]+–NH3 6/15, 40% 9/15, 60% a
[d-Ala2,d-Leu5]-enkephalin, 5 YADGFLD 4–5 3–5 2–5 5/5, 100% b 5/5, 100%
Met-enkephalin, 5 YGGFL [M – CH3SH]H+ 0/5, 0% 5/5, 100%

aSequence coverage achieved only through MS3 as MS/MS produced exclusively [M – H3PO4 + H3]3+.

bDetected fragment ions were all less than 1% abundance relative to the protonated molecular ion of the peptide.