Targeted proteome investigation via selected reaction monitoring mass spectrometry

被引:45
作者
Maiolica, Alessio [1 ]
Juenger, Martin A. [1 ]
Ezkurdia, Iakes [2 ]
Aebersold, Ruedi [1 ,3 ]
机构
[1] ETH, Inst Mol Syst Biol, Dept Biol, CH-8093 Zurich, Switzerland
[2] Spanish Natl Canc Res Ctr CNIO, Struct Biol & Biocomp Programme, Madrid, Spain
[3] Univ Zurich, Fac Sci, Zurich, Switzerland
基金
欧洲研究理事会; 瑞士国家科学基金会;
关键词
Selected Reaction Monitoring (SRM); Proteomics; Antibodies; Mass spectrometry; Proteome mapping; GENOME-WIDE ANALYSIS; QUANTITATIVE-ANALYSIS; SHOTGUN PROTEOMICS; SEQUENCE POLYMORPHISMS; STATISTICAL-MODEL; NEXT-GENERATION; HUMAN PATHOGEN; GENE NUMBER; PROTEINS; IDENTIFICATION;
D O I
10.1016/j.jprot.2012.04.048
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Due to the enormous complexity of proteomes which constitute the entirety of protein species expressed by a certain cell or tissue, proteome-wide studies performed in discovery mode are still limited in their ability to reproducibly identify and quantify all proteins present in complex biological samples. Therefore, the targeted analysis of informative subsets of the proteome has been beneficial to generate reproducible data sets across multiple samples. Here we review the repertoire of antibody- and mass spectrometry (MS) -based analytical tools which is currently available for the directed analysis of predefined sets of proteins. The topics of emphasis for this review are Selected Reaction Monitoring (SRM) mass spectrometry, emerging tools to control error rates in targeted proteomic experiments, and some representative examples of applications. The ability to cost- and time-efficiently generate specific and quantitative assays for large numbers of proteins and posttranslational modifications has the potential to greatly expand the range of targeted proteomic coverage in biological studies. This article is part of a Special Section entitled: Understanding genome regulation and genetic diversity by mass spectrometry. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:3495 / 3513
页数:19
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