A comprehensive investigation of proline fragmentation behavior in low-energy collision-induced dissociation peptide mass spectra

被引:13
|
作者
Dong, Nai-ping [1 ]
Zhang, Liang-xiao [1 ]
Liang, Yi-zeng [1 ]
机构
[1] Cent S Univ, Coll Chem & Engn, Changsha 410083, Peoples R China
关键词
Proline effect; Protonated peptides; Proline fragmentation map; Specific cleavage effect; Statistical analysis; PROTONATED PEPTIDES; STATISTICAL CHARACTERIZATION; ELECTROSPRAY-IONIZATION; SPECTROMETRY; CLEAVAGE; DEPENDENCE; HISTIDINE; PATHWAYS; PROTEINS; DATABASE;
D O I
10.1016/j.ijms.2011.08.005
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
An investigation of more than 130000 tandem mass spectra of praline-containing peptides extracted from Human and Ecoli peptide libraries in NIST Libraries (http://peptide.nist.gov/) is presented. In this study, fragmentation maps are drawn to show the fragmentation behavior of praline (Pro) in protonated peptides, taking the factors affecting the cleavage N-terminal to Pro as points of the map. In order to quantitatively characterize the fragmentation behavior of proline, probability of occurring selective cleavage at N-terminal side of Pro for each point is calculated. From the fragmentation maps, selective cleavage at N-terminal side of Pro is suppressed when all protons are sequestered by Args except at Asp-Pro and Glu-Pro. When protons are mobile, cleavage at N-terminal side of Pro is determined by pairwise cleavage Xxx-Pro and positions of praline in peptides. For triply and quadruply charged peptides, the Coulombic repulsion between protons affects the fragmentation of peptides and subsequently suppresses the cleavage at N-terminal side of Pro. Other fragmentation pathways influencing the fragmentation such as aspartic acid effect and y(N-2)/b(2) pathway are also found. Investigation of multiple praline containing peptides shows similar influential factors and competition between multiple prolines. (C) 2011 Published by Elsevier B.V.
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页码:89 / 97
页数:9
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