Cysteine Oxidative Posttranslational Modifications Emerging Regulation in the Cardiovascular System

被引:237
作者
Chung, Heaseung S. [1 ]
Wang, Sheng-Bing [2 ]
Venkatraman, Vidya [2 ,3 ]
Murray, Christopher I. [1 ]
Van Eyk, Jennifer E. [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Dept Biol Chem, Baltimore, MD 21224 USA
[2] Johns Hopkins Univ, Dept Med, Baltimore, MD 21224 USA
[3] Johns Hopkins Univ, Bayview Prote Ctr, Baltimore, MD 21224 USA
关键词
cardiac protection; cysteine oxidative posttranslational modification; heart failure; protein; redox-switches; OXIDANT-SENSITIVE PROTEINS; S-NITROSYLATION; REDOX REGULATION; SULFENIC ACID; ATP SYNTHASE; SIGNAL-TRANSDUCTION; HYDROGEN-SULFIDE; BETA-ACTIN; IDENTIFICATION; GLUTATHIONYLATION;
D O I
10.1161/CIRCRESAHA.112.268680
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
In the cardiovascular system, changes in oxidative balance can affect many aspects of cellular physiology through redox-signaling. Depending on the magnitude, fluctuations in the cell's production of reactive oxygen and nitrogen species can regulate normal metabolic processes, activate protective mechanisms, or be cytotoxic. Reactive oxygen and nitrogen species can have many effects including the posttranslational modification of proteins at critical cysteine thiols. A subset can act as redox-switches, which elicit functional effects in response to changes in oxidative state. Although the general concepts of redox-signaling have been established, the identity and function of many regulatory switches remains unclear. Characterizing the effects of individual modifications is the key to understand how the cell interprets oxidative signals under physiological and pathological conditions. Here, we review the various cysteine oxidative posttranslational modifications and their ability to function as redox-switches that regulate the cell's response to oxidative stimuli. In addition, we discuss how these modifications have the potential to influence other posttranslational modifications' signaling pathways though cross-talk. Finally, we review the increasing number of tools being developed to identify and quantify the various cysteine oxidative posttranslational modifications and how this will advance our understanding of redox-regulation. (Circ Res. 2013;112:382-392.)
引用
收藏
页码:382 / 392
页数:11
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