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- W2164377269 endingPage "1204" @default.
- W2164377269 startingPage "1189" @default.
- W2164377269 abstract "Disulfide bond formation is a crucial step for oxidative folding and necessary for the acquisition of a protein's native conformation. Introduction of disulfide bonds is catalyzed in specialized subcellular compartments and requires the coordinated action of specific enzymes. The intermembrane space of mitochondria has recently been found to harbor a dedicated machinery that promotes the oxidative folding of substrate proteins by shuttling disulfide bonds. The newly identified oxidative pathway consists of the redox-regulated receptor Mia40 and the sulfhydryl oxidase Erv1. Proteins destined to the intermembrane space are trapped by a disulfide relay mechanism that involves an electron cascade from the incoming substrate to Mia40, then on to Erv1, and finally to molecular oxygen via cytochrome c. This thiol-disulfide exchange mechanism is essential for the import and for maintaining the structural stability of the incoming precursors. In this review we describe the mechanistic parameters that define the interaction and oxidation of the substrate proteins in light of the recent publications in the mitochondrial oxidative folding field." @default.
- W2164377269 created "2016-06-24" @default.
- W2164377269 creator A5065474092 @default.
- W2164377269 creator A5068554597 @default.
- W2164377269 date "2010-10-15" @default.
- W2164377269 modified "2023-09-23" @default.
- W2164377269 title "Oxidative Protein Folding in the Mitochondrial Intermembrane Space" @default.
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