Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1782313416455618560 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3998802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ruggianoannamaria erassociateddegradationproteinqualitycontrolandbeyond AT forestiombretta erassociateddegradationproteinqualitycontrolandbeyond AT carvalhopedro erassociateddegradationproteinqualitycontrolandbeyond |