Mass spectrometry-based proteomics: qualitative identification to activity-based protein profiling

被引:11
作者
Cardoza, Job D. [1 ,2 ]
Parikh, Jignesh R. [1 ,3 ]
Ficarro, Scott B. [1 ,2 ,4 ]
Marto, Jarrod A. [1 ,2 ,4 ]
机构
[1] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[3] Boston Univ, Bioinformat Program, Boston, MA 02215 USA
[4] Dana Farber Canc Inst, Blais Prote Ctr, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
ELECTRON-TRANSFER DISSOCIATION; CODED AFFINITY TAGS; HYDROPHILIC INTERACTION CHROMATOGRAPHY; COLLISION-INDUCED DISSOCIATION; ENZYME-ACTIVITY PROFILES; EMBRYONIC STEM-CELLS; FREE CLICK CHEMISTRY; LINEAR ION-TRAP; TYROSINE PHOSPHORYLATION; PHOSPHOPROTEOME ANALYSIS;
D O I
10.1002/wsbm.166
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Mass spectrometry has become the method of choice for proteome characterization, including multicomponent protein complexes (typically tens to hundreds of proteins) and total protein expression (up to tens of thousands of proteins), in biological samples. Qualitative sequence assignment based on MS/MS spectra is relatively well-defined, while statistical metrics for relative quantification have not completely stabilized. Nonetheless, proteomics studies have progressed to the point whereby various gene-, pathway-, or network-oriented computational frameworks may be used to place mass spectrometry data into biological context. Despite this progress, the dynamic range of protein expression remains a significant hurdle, and impedes comprehensive proteome analysis. Methods designed to enrich specific protein classes have emerged as an effective means to characterize enzymes or other catalytically active proteins that are otherwise difficult to detect in typical discovery mode proteomics experiments. Collectively, these approaches will facilitate identification of biomarkers and pathways relevant to diagnosis and treatment of human disease. WIREs Syst Biol Med 2012, 4:141162. doi: 10.1002/wsbm.166
引用
收藏
页码:141 / 162
页数:22
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