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Protein trafficking in the mitochondrial intermembrane space: mechanisms and links to human disease
Mitochondria fulfill a diverse range of functions in cells including oxygen metabolism, homeostasis of inorganic ions and execution of apoptosis. Biogenesis of mitochondria relies on protein import pathways that are ensured by dedicated multiprotein translocase complexes localized in all sub-compart...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509380/ https://www.ncbi.nlm.nih.gov/pubmed/28701417 http://dx.doi.org/10.1042/BCJ20160627 |
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author | MacPherson, Lisa Tokatlidis, Kostas |
author_facet | MacPherson, Lisa Tokatlidis, Kostas |
author_sort | MacPherson, Lisa |
collection | PubMed |
description | Mitochondria fulfill a diverse range of functions in cells including oxygen metabolism, homeostasis of inorganic ions and execution of apoptosis. Biogenesis of mitochondria relies on protein import pathways that are ensured by dedicated multiprotein translocase complexes localized in all sub-compartments of these organelles. The key components and pathways involved in protein targeting and assembly have been characterized in great detail over the last three decades. This includes the oxidative folding machinery in the intermembrane space, which contributes to the redox-dependent control of proteostasis. Here, we focus on several components of this system and discuss recent evidence suggesting links to human proteopathy. |
format | Online Article Text |
id | pubmed-5509380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55093802017-07-26 Protein trafficking in the mitochondrial intermembrane space: mechanisms and links to human disease MacPherson, Lisa Tokatlidis, Kostas Biochem J Review Articles Mitochondria fulfill a diverse range of functions in cells including oxygen metabolism, homeostasis of inorganic ions and execution of apoptosis. Biogenesis of mitochondria relies on protein import pathways that are ensured by dedicated multiprotein translocase complexes localized in all sub-compartments of these organelles. The key components and pathways involved in protein targeting and assembly have been characterized in great detail over the last three decades. This includes the oxidative folding machinery in the intermembrane space, which contributes to the redox-dependent control of proteostasis. Here, we focus on several components of this system and discuss recent evidence suggesting links to human proteopathy. Portland Press Ltd. 2017-08-01 2017-07-12 /pmc/articles/PMC5509380/ /pubmed/28701417 http://dx.doi.org/10.1042/BCJ20160627 Text en © 2017 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Articles MacPherson, Lisa Tokatlidis, Kostas Protein trafficking in the mitochondrial intermembrane space: mechanisms and links to human disease |
title | Protein trafficking in the mitochondrial intermembrane space: mechanisms and links to human disease |
title_full | Protein trafficking in the mitochondrial intermembrane space: mechanisms and links to human disease |
title_fullStr | Protein trafficking in the mitochondrial intermembrane space: mechanisms and links to human disease |
title_full_unstemmed | Protein trafficking in the mitochondrial intermembrane space: mechanisms and links to human disease |
title_short | Protein trafficking in the mitochondrial intermembrane space: mechanisms and links to human disease |
title_sort | protein trafficking in the mitochondrial intermembrane space: mechanisms and links to human disease |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509380/ https://www.ncbi.nlm.nih.gov/pubmed/28701417 http://dx.doi.org/10.1042/BCJ20160627 |
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