Oxidative Folding in the Mitochondrial Intermembrane Space in Human Health and Disease

被引:7
|
作者
Fraga, Hugo [1 ]
Ventura, Salvador [1 ,2 ]
机构
[1] Autonomous Univ Barcelona, Dept Biochem & Mol Biol, E-08193 Bellaterra, Spain
[2] Autonomous Univ Barcelona, Inst Biotechnol & Biomed, E-08193 Bellaterra, Spain
关键词
cysteine motifs; disulfide bonds; Erv1; intermembrane space; Mia40; mitochondria; oxidative protein folding; protein import; oxidative stress; DISULFIDE RELAY SYSTEM; PROTEIN IMPORT; COPPER CHAPERONE; SUPEROXIDE-DISMUTASE; CU; ZN-SUPEROXIDE DISMUTASE; CRYSTAL-STRUCTURE; MIA40; SOD1; METALLOCHAPERONE; TRANSLOCATION;
D O I
10.3390/ijms14022916
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
Oxidative folding in the mitochondrial intermembrane space (IMS) is a key cellular event associated with the folding and import of a large and still undetermined number of proteins. This process is catalyzed by an oxidoreductase, Mia40 that is able to recognize substrates with apparently little or no homology. Following substrate oxidation, Mia40 is reduced and must be reoxidized by Erv1/Alr1 that consequently transfers the electrons to the mitochondrial respiratory chain. Although our understanding of the physiological relevance of this process is still limited, an increasing number of pathologies are being associated with the impairment of this pathway; especially because oxidative folding is fundamental for several of the proteins involved in defense against oxidative stress. Here we review these aspects and discuss recent findings suggesting that oxidative folding in the IMS is modulated by the redox state of the cell.
引用
收藏
页码:2916 / 2927
页数:12
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