Cysteine-Based Redox Switches in Enzymes

被引:292
作者
Klomsiri, Chananat [1 ]
Karplus, P. Andrew [2 ]
Poole, Leslie B. [1 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Biochem, Winston Salem, NC 27157 USA
[2] Oregon State Univ, Dept Biochem & Biophys, Corvallis, OR 97331 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
PROTEIN-TYROSINE PHOSPHATASES; DISULFIDE BOND FORMATION; SULFENIC ACID FORMATION; NEURONAL CELL-DEATH; OXIDATIVE STRESS; HYDROGEN-PEROXIDE; HYPOCHLOROUS ACID; IN-VIVO; REVERSIBLE INACTIVATION; BACTERIAL PEROXIREDOXIN;
D O I
10.1089/ars.2010.3376
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
The enzymes involved in metabolism and signaling are regulated by posttranslational modifications that influence their catalytic activity, rates of turnover, and targeting to subcellular locations. Most prominent among these has been phosphorylation/dephosphorylation, but now a distinct class of modification coming to the fore is a set of versatile redox modifications of key cysteine residues. Here we review the chemical, structural, and regulatory aspects of such redox regulation of enzymes and discuss examples of how these regulatory modifications often work in concert with phosphorylation/dephosphorylation events, making redox dependence an integral part of many cell signaling processes. Included are the emerging roles played by peroxiredoxins, a family of cysteine-based peroxidases that now appear to be major players in both antioxidant defense and cell signaling. Antioxid. Redox Signal. 14, 1065-1077.
引用
收藏
页码:1065 / 1077
页数:13
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