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ER-associated degradation: Protein quality control and beyond

Even with the assistance of many cellular factors, a significant fraction of newly synthesized proteins ends up misfolded. Cells evolved protein quality control systems to ensure that these potentially toxic species are detected and eliminated. The best characterized of these pathways, the ER-associ...

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Detalles Bibliográficos
Autores principales: Ruggiano, Annamaria, Foresti, Ombretta, Carvalho, Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998802/
https://www.ncbi.nlm.nih.gov/pubmed/24637321
http://dx.doi.org/10.1083/jcb.201312042
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author Ruggiano, Annamaria
Foresti, Ombretta
Carvalho, Pedro
author_facet Ruggiano, Annamaria
Foresti, Ombretta
Carvalho, Pedro
author_sort Ruggiano, Annamaria
collection PubMed
description Even with the assistance of many cellular factors, a significant fraction of newly synthesized proteins ends up misfolded. Cells evolved protein quality control systems to ensure that these potentially toxic species are detected and eliminated. The best characterized of these pathways, the ER-associated protein degradation (ERAD), monitors the folding of membrane and secretory proteins whose biogenesis takes place in the endoplasmic reticulum (ER). There is also increasing evidence that ERAD controls other ER-related functions through regulated degradation of certain folded ER proteins, further highlighting the role of ERAD in cellular homeostasis.
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spelling pubmed-39988022014-09-17 ER-associated degradation: Protein quality control and beyond Ruggiano, Annamaria Foresti, Ombretta Carvalho, Pedro J Cell Biol Reviews Even with the assistance of many cellular factors, a significant fraction of newly synthesized proteins ends up misfolded. Cells evolved protein quality control systems to ensure that these potentially toxic species are detected and eliminated. The best characterized of these pathways, the ER-associated protein degradation (ERAD), monitors the folding of membrane and secretory proteins whose biogenesis takes place in the endoplasmic reticulum (ER). There is also increasing evidence that ERAD controls other ER-related functions through regulated degradation of certain folded ER proteins, further highlighting the role of ERAD in cellular homeostasis. The Rockefeller University Press 2014-03-17 /pmc/articles/PMC3998802/ /pubmed/24637321 http://dx.doi.org/10.1083/jcb.201312042 Text en © 2014 Ruggiano et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Reviews
Ruggiano, Annamaria
Foresti, Ombretta
Carvalho, Pedro
ER-associated degradation: Protein quality control and beyond
title ER-associated degradation: Protein quality control and beyond
title_full ER-associated degradation: Protein quality control and beyond
title_fullStr ER-associated degradation: Protein quality control and beyond
title_full_unstemmed ER-associated degradation: Protein quality control and beyond
title_short ER-associated degradation: Protein quality control and beyond
title_sort er-associated degradation: protein quality control and beyond
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998802/
https://www.ncbi.nlm.nih.gov/pubmed/24637321
http://dx.doi.org/10.1083/jcb.201312042
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