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Radical Stability Directs Electron Capture and Transfer Dissociation of β‐Amino Acids in Peptides
Author(s) -
Ben Hamidane Hisham,
Vorobyev Aleksey,
Larregola Maud,
Lukaszuk Aneta,
Tourwé Dirk,
Lavielle Solange,
Karoyan Philippe,
Tsybin Yury O.
Publication year - 2010
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.200902480
Subject(s) - chemistry , amino acid , side chain , electron capture dissociation , peptide , deamidation , dissociation (chemistry) , tandem mass spectrometry , peptide bond , electron transfer dissociation , stereochemistry , mass spectrometry , organic chemistry , biochemistry , enzyme , chromatography , polymer
We report on the characteristics of the radical‐ion‐driven dissociation of a diverse array of β‐amino acids incorporated into α‐peptides, as probed by tandem electron‐capture and electron‐transfer dissociation (ECD/ETD) mass spectrometry. The reported results demonstrate a stronger ECD/ETD dependence on the nature of the amino acid side chain for β‐amino acids than for their α‐form counterparts. In particular, only aromatic (e.g., β‐Phe), and to a substantially lower extent, carbonyl‐containing (e.g., β‐Glu and β‐Gln) amino acid side chains, lead to NC β bond cleavage in the corresponding β‐amino acids. We conclude that radical stabilization must be provided by the side chain to enable the radical‐driven fragmentation from the nearby backbone carbonyl carbon to proceed. In contrast with the cleavage of backbones derived from α‐amino acids, ECD of peptides composed mainly of β‐amino acids reveals a shift in cleavage priority from the NC β to the C α C bond. The incorporation of CH 2 groups into the peptide backbone may thus drastically influence the backbone charge solvation preference. The characteristics of radical‐driven β‐amino acid dissociation described herein are of particular importance to methods development, applications in peptide sequencing, and peptide and protein modification (e.g., deamidation and isomerization) analysis in life science research.