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The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis

The three mitochondrial-encoded proteins, COX1, COX2, and COX3, form the core of the cytochrome c oxidase. Upon synthesis, COX2 engages with COX20 in the inner mitochondrial membrane, a scaffold protein that recruits metallochaperones for copper delivery to the Cu(A)-Site of COX2. Here we identified...

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Autores principales: Lorenzi, Isotta, Oeljeklaus, Silke, Aich, Abhishek, Ronsör, Christin, Callegari, Sylvie, Dudek, Jan, Warscheid, Bettina, Dennerlein, Sven, Rehling, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Pub. Co 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5764226/
https://www.ncbi.nlm.nih.gov/pubmed/29154948
http://dx.doi.org/10.1016/j.bbamcr.2017.11.010
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author Lorenzi, Isotta
Oeljeklaus, Silke
Aich, Abhishek
Ronsör, Christin
Callegari, Sylvie
Dudek, Jan
Warscheid, Bettina
Dennerlein, Sven
Rehling, Peter
author_facet Lorenzi, Isotta
Oeljeklaus, Silke
Aich, Abhishek
Ronsör, Christin
Callegari, Sylvie
Dudek, Jan
Warscheid, Bettina
Dennerlein, Sven
Rehling, Peter
author_sort Lorenzi, Isotta
collection PubMed
description The three mitochondrial-encoded proteins, COX1, COX2, and COX3, form the core of the cytochrome c oxidase. Upon synthesis, COX2 engages with COX20 in the inner mitochondrial membrane, a scaffold protein that recruits metallochaperones for copper delivery to the Cu(A)-Site of COX2. Here we identified the human protein, TMEM177 as a constituent of the COX20 interaction network. Loss or increase in the amount of TMEM177 affects COX20 abundance leading to reduced or increased COX20 levels respectively. TMEM177 associates with newly synthesized COX2 and SCO2 in a COX20-dependent manner. Our data shows that by unbalancing the amount of TMEM177, newly synthesized COX2 accumulates in a COX20-associated state. We conclude that TMEM177 promotes assembly of COX2 at the level of Cu(A)-site formation.
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spelling pubmed-57642262018-02-01 The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis Lorenzi, Isotta Oeljeklaus, Silke Aich, Abhishek Ronsör, Christin Callegari, Sylvie Dudek, Jan Warscheid, Bettina Dennerlein, Sven Rehling, Peter Biochim Biophys Acta Article The three mitochondrial-encoded proteins, COX1, COX2, and COX3, form the core of the cytochrome c oxidase. Upon synthesis, COX2 engages with COX20 in the inner mitochondrial membrane, a scaffold protein that recruits metallochaperones for copper delivery to the Cu(A)-Site of COX2. Here we identified the human protein, TMEM177 as a constituent of the COX20 interaction network. Loss or increase in the amount of TMEM177 affects COX20 abundance leading to reduced or increased COX20 levels respectively. TMEM177 associates with newly synthesized COX2 and SCO2 in a COX20-dependent manner. Our data shows that by unbalancing the amount of TMEM177, newly synthesized COX2 accumulates in a COX20-associated state. We conclude that TMEM177 promotes assembly of COX2 at the level of Cu(A)-site formation. Elsevier Pub. Co 2018-02 /pmc/articles/PMC5764226/ /pubmed/29154948 http://dx.doi.org/10.1016/j.bbamcr.2017.11.010 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Lorenzi, Isotta
Oeljeklaus, Silke
Aich, Abhishek
Ronsör, Christin
Callegari, Sylvie
Dudek, Jan
Warscheid, Bettina
Dennerlein, Sven
Rehling, Peter
The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis
title The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis
title_full The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis
title_fullStr The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis
title_full_unstemmed The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis
title_short The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis
title_sort mitochondrial tmem177 associates with cox20 during cox2 biogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5764226/
https://www.ncbi.nlm.nih.gov/pubmed/29154948
http://dx.doi.org/10.1016/j.bbamcr.2017.11.010
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