Subcellular Redox Targeting: Bridging in Vitro and in Vivo Chemical Biology

被引:22
|
作者
Long, Marcus J. C. [1 ]
Poganik, Jesse R. [1 ]
Ghosh, Souradyuti [1 ]
Aye, Yimon [1 ,2 ]
机构
[1] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14850 USA
[2] Weill Cornell Med, Dept Biochem, New York, NY 10065 USA
基金
美国国家科学基金会;
关键词
ASSISTED LIGHT INACTIVATION; CYSTEINE SULFENIC ACID; INTRACELLULAR HYDROGEN-PEROXIDE; SITE-SPECIFIC ANALYSIS; REACTIVE OXYGEN; FLUORESCENT PROTEIN; OXIDATIVE STRESS; ELECTROPHILIC MODIFICATIONS; LIPID OXIDATION; SINGLET OXYGEN;
D O I
10.1021/acschembio.6b01148
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
Networks of redox sensor proteins within discrete microdomains regulate the flow of redox signaling. Yet, the inherent reactivity of redox signals complicates the study of specific redox events and pathways by traditional methods. Herein, we review designer chemistries capable of measuring flux and/or mimicking subcellular redox signaling at the cellular and organismal level. Such efforts have begun to decipher the logic underlying organelle-, site-, and target-specific redox signaling in vitro and in vivo. These data highlight chemical biology as a perfect gateway to interrogate how nature choreographs subcellular redox chemistry to drive precision redox biology.
引用
收藏
页码:586 / 600
页数:15
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