Proteomics and Beyond: Cell Decision-Making Shaped by Reactive Electrophiles

被引:34
作者
Liu, Xuyu [1 ,2 ]
Long, Marcus J. C. [2 ]
Aye, Yimon [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, CH-1015 Lausanne, Switzerland
[2] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
4-HYDROXY-2(E)-NONENAL ENANTIOMERS; REDOX; NRF2; DISCOVERY; TARGETS; DETOXIFICATION; CONSEQUENCES; ALKYLATION; ADDUCTION; BIOLOGY;
D O I
10.1016/j.tibs.2018.09.014
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
Revolutionary proteomic strategies have enabled rapid profiling of the cellular targets of electrophilic small molecules. However, precise means to directly interrogate how these individual electrophilic modifications at low occupancy functionally reshape signaling networks have until recently been largely limited. We highlight here new methods that transcend proteomic platforms to forge a quantitative link between protein target-selective engagement and downstream signaling. We focus on recent progress in the study of non-enzyme-assisted signaling mechanisms and crosstalk choreographed by native reactive electrophilic species (RES). Using this as a model, we offer a long-term vision of how these toolsets together with fundamental biochemical knowledge of precision electrophile signaling may be harnessed to assist covalent ligand-target matching and ultimately amend disease-specific signaling dysfunction.
引用
收藏
页码:75 / 89
页数:15
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