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The Mitochondrial Disulfide Relay System: Roles in Oxidative Protein Folding and Beyond
Author(s) -
M. Dominik Fischer,
Jan Riemer
Publication year - 2013
Publication title -
international journal of cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.587
H-Index - 53
eISSN - 1687-8884
pISSN - 1687-8876
DOI - 10.1155/2013/742923
Subject(s) - mitochondrial intermembrane space , disulfide bond , oxidative folding , intermembrane space , mitochondrion , microbiology and biotechnology , protein folding , biochemistry , oxidative phosphorylation , biology , protein disulfide isomerase , chemistry , gene , escherichia coli , bacterial outer membrane
Disulfide bond formation drives protein import of most proteins of the mitochondrial intermembrane space (IMS). The main components of this disulfide relay machinery are the oxidoreductase Mia40 and the sulfhydryl oxidase Erv1/ALR. Their precise functions have been elucidated in molecular detail for the yeast and human enzymes in vitro and in intact cells. However, we still lack knowledge on how Mia40 and Erv1/ALR impact cellular and organism physiology and whether they have functions beyond their role in disulfide bond formation. Here we summarize the principles of oxidation-dependent protein import mediated by the mitochondrial disulfide relay. We proceed by discussing recently described functions of Mia40 in the hypoxia response and of ALR in influencing mitochondrial morphology and its importance for tissue development and embryogenesis. We also include a discussion of the still mysterious function of Erv1/ALR in liver regeneration.

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