High resolution data-independent acquisition with electron transfer dissociation mass spectrometry: Multiplexed analysis of post-translationally modified proteins

被引:2
|
作者
Sweredoski, Michael J. [1 ]
Second, Tonya Pekar [2 ]
Broeker, Jenny [3 ]
Moradian, Annie [1 ]
Hess, Sonja [1 ]
机构
[1] CALTECH, Beckman Inst, Proteome Explorat Lab, Div Biol & Biol Engn, Pasadena, CA 91125 USA
[2] Thermo Sci, San Jose, CA 95134 USA
[3] Heidelberg Univ, Inst Pharmacol, D-69120 Heidelberg, Germany
关键词
Middle-down proteomics; ETD; Electron transfer dissociation; Histone; High resolution; Data-independent acquisition; INFRARED MULTIPHOTON DISSOCIATION; CAPTURE DISSOCIATION; MIDDLE-DOWN; TOP-DOWN; QUANTITATIVE PROTEOMICS; PEPTIDE; PHOSPHORYLATION; HISTONES; MS/MS; IDENTIFICATION;
D O I
10.1016/j.ijms.2015.06.018
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
Data-dependent acquisition (DDA) mode is the most commonly used method in bottom-up proteomics. Recently, data-independent acquisition (DIA) modes have become popular alternatives because of their unbiased analysis, leading in general to more comprehensive, global qualitative profiling of proteome systems and also higher quantitative reproducibility in such profiling. Most of the previously established DIA methods are based on collision-induced dissociation (CID). However, when it comes to the analysis of labile post-translational modifications (PTMs), electron capture/transfer dissociation (ECD/ETD) may be better suited. In addition to the bottom-up approach, the middle-down approach, which analyzes peptides in the range of 3,000-10,000 Da has emerged as an attractive alternative, including the analysis of highly modified and highly variable protein variants that exist in key system functions, such as histone signaling cascades. Here, we establish that a data-independent (DIA) middle-down ETD approach is a superior strategy in the differential characterization of PTM changes in histone H2B. We suggest that this strategy can further be used for other approaches where dynamic PTM characterization or changes due to different conditions are fundamental to accurate understanding of biological systems and function, (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:155 / 162
页数:8
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