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Structural heterogeneity of doubly-charged peptide b-Ions
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Li, Xiaojuan, Huang, Yiqun, O’Connor, Peter B. and Lin, Cheng. (2011) Structural heterogeneity of doubly-charged peptide b-Ions. Journal of The American Society for Mass Spectrometry, Vol.22 (No.2). pp. 245-254. ISSN 1044-0305
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Official URL: http://dx.doi.org/10.1007/s13361-010-0036-1
Abstract
Performing collisionally activated dissociation (CAD) and electron capture dissociation (ECD) in tandem has shown great promise in providing comprehensive sequence information that was otherwise unobtainable by using either fragmentation method alone or in duet. However, the general applicability of this MS3 approach in peptide sequencing may be undermined by the formation of non-direct sequence ions, as sometimes observed under CAD, particularly when multiple stages of CAD are involved. In this study, varied-sized doubly-charged b-ions from three tachykinin peptides were investigated by ECD. Sequence scrambling was observed in ECD of all b-ions from neurokinin A (HKTDSFVGLM-NH2), suggesting the presence of N- and C-termini linked macro-cyclic conformers. On the contrary, none of the b-ions from eledoisin (pEPSKDAFIGLM-NH2) produced non-direct sequence ions under ECD, as it does not contain a free N-terminal amino group. ECD of several b-ions from Substance P (RPKPQQFFGLM-NH2) showed series of cm-Lys fragment ions which suggested that the macro-cyclic structure may also be formed by connecting the C-terminal carbonyl group and the ε-amino group of the lysine side chain. Theoretical investigation of selected Substance P b-ions revealed several low energy conformers, including both linear oxazolones and macro-ring structures, in corroboration with the experimental observation. This study showed that a b-ion may exist as a mixture of several forms, with their propensities influenced by its N-terminus, length, and certain side-chain groups. Further, the presence of several macro-cyclic structures may result in erroneous sequence assignment when the combined CAD and ECD methods are used in peptide sequencing.
| Item Type: | Journal Article |
|---|---|
| Subjects: | Q Science > QD Chemistry Q Science > QP Physiology |
| Divisions: | Faculty of Science > Chemistry |
| Library of Congress Subject Headings (LCSH): | Amino acid sequence, Tachykinins, Tandem mass spectrometry |
| Journal or Publication Title: | Journal of The American Society for Mass Spectrometry |
| Publisher: | Springer New York LLC |
| ISSN: | 1044-0305 |
| Date: | February 2011 |
| Volume: | Vol.22 |
| Number: | No.2 |
| Number of Pages: | 10 |
| Page Range: | pp. 245-254 |
| Identification Number: | 10.1007/s13361-010-0036-1 |
| Status: | Peer Reviewed |
| Publication Status: | Published |
| Access rights to Published version: | Restricted or Subscription Access |
| Funder: | National Institutes of Health (U.S.) (NIH), National Center for Research Resources (U.S.) (NCRR), National Heart, Lung, and Blood Institute (NHLBI), National Institute of General Medical Sciences (U.S.) (NIGMS) |
| Grant number: | P41RR10888 (NIH/NCRR), S10RR025082 (NIH/NCRR), N01HV28178 (NIH/NHLBI), R01GM078293 (NIH/NIGMS) |
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| URI: | http://wrap.warwick.ac.uk/id/eprint/40597 |
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