Proteomics approaches to decipher new signaling pathways

被引:6
作者
Gingras, Anne-Claude [1 ,2 ]
Wong, Cassandra J. J. [1 ,2 ]
机构
[1] Lunenfeld Tanenbaum Res Inst, Toronto, ON, Canada
[2] Univ Toronto, Dept Mol Genet, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
LIVE MAMMALIAN-CELLS; LARGE-SCALE ANALYSIS; MASS-SPECTROMETRY; PROTEIN-KINASE; QUANTITATIVE PROTEOMICS; HIGH-RESOLUTION; REVEALS; PHOSPHORYLATION; YEAST; PHOSPHOPROTEOMICS;
D O I
10.1016/j.sbi.2016.07.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cells have evolved intricate ways to propagate signals through signaling networks rich in crosstalks between signaling pathways and feedforward and feedback loops. The enzymatic products of phosphorylation-dependent signaling, namely phosphopeptides, can be identified and quantified systematically by mass spectrometry. Recent advances in the speed and sensitivity of mass spectrometers, combined with improvements in sample preparation and data analysis, are enabling the acquisition of increasingly large phosphopeptide datasets. Here, we discuss several considerations in experimental design that aid in unraveling direct and indirect phosphorylation events, as well as to identify crosstalks and feedback loops.
引用
收藏
页码:128 / 134
页数:7
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