Mitochondrial Respiratory Complex I: Structure, Function and Implication in Human Diseases

被引:306
作者
Sharma, Lokendra K. [1 ]
Lu, Jianxin [2 ]
Bai, Yidong [1 ,2 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Dept Cellular & Struct Biol, San Antonio, TX 78229 USA
[2] Wenzhou Med Coll, Zhejiang Prov Key Lab Med Genet, Sch Lab Med, Sch Life Sci, Wenzhou 325035, Peoples R China
基金
美国国家卫生研究院;
关键词
Mitochondria; complex I; oxidative stress; reactive oxygen species; apoptosis; complex I functions; NADH-UBIQUINONE OXIDOREDUCTASE; HEREDITARY OPTIC NEUROPATHY; DNA-ENCODED SUBUNITS; ACYL CARRIER PROTEIN; 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE MOUSE MODEL; POLYACRYLAMIDE-GEL ELECTROPHORESIS; BOVINE HEART-MITOCHONDRIA; APOPTOSIS-INDUCING FACTOR; ELECTRON-TRANSPORT CHAIN; CYTOCHROME-C-OXIDASE;
D O I
10.2174/092986709787846578
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
Mitochondria are ubiquitous organelles in eukaryotic cells whose primary function is to generate energy supplies in the form of ATP through oxidative phosphorylation. As the entry point for most electrons into the respiratory chain, NADH: ubiquinone oxidoreductase, or complex I, is the largest and least understood component of the mitochondrial oxidative phosphorylation system. Substantial progress has been made in recent years in understanding its subunit composition, its assembly, the interaction among complex I and other respiratory components, and its role in oxidative stress and apoptosis. This review provides an updated overview of the structure of complex I, as well as its cellular functions, and discusses the implication of complex I dysfunction in various human diseases.
引用
收藏
页码:1266 / 1277
页数:12
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