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

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 n...

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Detalles Bibliográficos
Autores principales: Fraga, Hugo, Ventura, Salvador
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588022/
https://www.ncbi.nlm.nih.gov/pubmed/23364613
http://dx.doi.org/10.3390/ijms14022916
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author Fraga, Hugo
Ventura, Salvador
author_facet Fraga, Hugo
Ventura, Salvador
author_sort Fraga, Hugo
collection PubMed
description 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.
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spelling pubmed-35880222013-03-13 Oxidative Folding in the Mitochondrial Intermembrane Space in Human Health and Disease Fraga, Hugo Ventura, Salvador Int J Mol Sci Review 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. MDPI 2013-01-30 /pmc/articles/PMC3588022/ /pubmed/23364613 http://dx.doi.org/10.3390/ijms14022916 Text en © 2013 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Fraga, Hugo
Ventura, Salvador
Oxidative Folding in the Mitochondrial Intermembrane Space in Human Health and Disease
title Oxidative Folding in the Mitochondrial Intermembrane Space in Human Health and Disease
title_full Oxidative Folding in the Mitochondrial Intermembrane Space in Human Health and Disease
title_fullStr Oxidative Folding in the Mitochondrial Intermembrane Space in Human Health and Disease
title_full_unstemmed Oxidative Folding in the Mitochondrial Intermembrane Space in Human Health and Disease
title_short Oxidative Folding in the Mitochondrial Intermembrane Space in Human Health and Disease
title_sort oxidative folding in the mitochondrial intermembrane space in human health and disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588022/
https://www.ncbi.nlm.nih.gov/pubmed/23364613
http://dx.doi.org/10.3390/ijms14022916
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