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Sequencing of the thirteen structurally isomeric quartets of N‐terminal dipeptide motifs in peptides by collision‐induced dissociation
Author(s) -
Winter Dominic,
Lehmann Wolf D.
Publication year - 2009
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.200800628
Subject(s) - protonation , ion , chemistry , dissociation (chemistry) , dipeptide , stereochemistry , peptide , collision induced dissociation , mass spectrometry , crystallography , tandem mass spectrometry , chromatography , biochemistry , organic chemistry
N‐terminal sequencing of protonated peptides is challenging, since each b 2 ion represents two sequence isomers, e.g ., NE and EN. Additionally the occurrence of compositional isomers, such as NE and QD, further increases the number of isomers to four (NE, EN, QD, DQ). This leads to a subset of 13 b 2 ion masses where each value represents four individual species. The b 2 ions within such a quartet are characterized by the same elemental composition. To test the utility of CID for differentiation of isomeric b 2 ions, the CID spectra of 52 small synthetic peptides were recorded, representing the 13 isomeric b 2 ion quartets, which may be formed from unmodified amino acid residues. The CID spectra of protonated peptides containing these quartets were carefully inspected for N‐terminal sequence information. Below the m / z value of the b 2 ion, individual differences were found in the b 2 fragment ion signatures (neutral loss of CO, H 2 O, NH 3 , and other less common units). Recognition of N and Q in second position from the N‐terminus is based on c 1 ion formation. Relative intensities of immonium ions were also used for differentiation between sequence isomers. In the complementary high‐mass regions above the m / z value of the y max‐2 ion, individual differences were observed in the formation of y max‐1 , x max‐1 and z max‐1 ions, which could be correlated to the complementary low‐mass ions. In summary, de novo sequencing of the N‐terminal dipeptide motif is feasible by considering all available sequence information present in CID spectra of protonated peptides.