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Oxidative protein biogenesis and redox regulation in the mitochondrial intermembrane space

Mitochondria are organelles that play a central role in cellular metabolism, as they are responsible for processes such as iron/sulfur cluster biogenesis, respiration and apoptosis. Here, we describe briefly the various protein import pathways for sorting of mitochondrial proteins into the different...

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Autores principales: Manganas, Phanee, MacPherson, Lisa, Tokatlidis, Kostas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203823/
https://www.ncbi.nlm.nih.gov/pubmed/27632163
http://dx.doi.org/10.1007/s00441-016-2488-5
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author Manganas, Phanee
MacPherson, Lisa
Tokatlidis, Kostas
author_facet Manganas, Phanee
MacPherson, Lisa
Tokatlidis, Kostas
author_sort Manganas, Phanee
collection PubMed
description Mitochondria are organelles that play a central role in cellular metabolism, as they are responsible for processes such as iron/sulfur cluster biogenesis, respiration and apoptosis. Here, we describe briefly the various protein import pathways for sorting of mitochondrial proteins into the different subcompartments, with an emphasis on the targeting to the intermembrane space. The discovery of a dedicated redox-controlled pathway in the intermembrane space that links protein import to oxidative protein folding raises important questions on the redox regulation of this process. We discuss the salient features of redox regulation in the intermembrane space and how such mechanisms may be linked to the more general redox homeostasis balance that is crucial not only for normal cell physiology but also for cellular dysfunction.
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spelling pubmed-52038232017-01-13 Oxidative protein biogenesis and redox regulation in the mitochondrial intermembrane space Manganas, Phanee MacPherson, Lisa Tokatlidis, Kostas Cell Tissue Res Review Mitochondria are organelles that play a central role in cellular metabolism, as they are responsible for processes such as iron/sulfur cluster biogenesis, respiration and apoptosis. Here, we describe briefly the various protein import pathways for sorting of mitochondrial proteins into the different subcompartments, with an emphasis on the targeting to the intermembrane space. The discovery of a dedicated redox-controlled pathway in the intermembrane space that links protein import to oxidative protein folding raises important questions on the redox regulation of this process. We discuss the salient features of redox regulation in the intermembrane space and how such mechanisms may be linked to the more general redox homeostasis balance that is crucial not only for normal cell physiology but also for cellular dysfunction. Springer Berlin Heidelberg 2016-09-08 2017 /pmc/articles/PMC5203823/ /pubmed/27632163 http://dx.doi.org/10.1007/s00441-016-2488-5 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Manganas, Phanee
MacPherson, Lisa
Tokatlidis, Kostas
Oxidative protein biogenesis and redox regulation in the mitochondrial intermembrane space
title Oxidative protein biogenesis and redox regulation in the mitochondrial intermembrane space
title_full Oxidative protein biogenesis and redox regulation in the mitochondrial intermembrane space
title_fullStr Oxidative protein biogenesis and redox regulation in the mitochondrial intermembrane space
title_full_unstemmed Oxidative protein biogenesis and redox regulation in the mitochondrial intermembrane space
title_short Oxidative protein biogenesis and redox regulation in the mitochondrial intermembrane space
title_sort oxidative protein biogenesis and redox regulation in the mitochondrial intermembrane space
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203823/
https://www.ncbi.nlm.nih.gov/pubmed/27632163
http://dx.doi.org/10.1007/s00441-016-2488-5
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