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Quality control at the plasma membrane: One mechanism does not fit all
The plasma membrane quality control system of eukaryotic cells is able to recognize and degrade damaged cell surface proteins. Recent studies have identified two mechanisms involved in the recognition of unfolded transmembrane proteins. One system uses chaperones to detect unfolded cytoplasmic domai...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Rockefeller University Press
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987138/ https://www.ncbi.nlm.nih.gov/pubmed/24733583 http://dx.doi.org/10.1083/jcb.201310113 |
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author | Babst, Markus |
author_facet | Babst, Markus |
author_sort | Babst, Markus |
collection | PubMed |
description | The plasma membrane quality control system of eukaryotic cells is able to recognize and degrade damaged cell surface proteins. Recent studies have identified two mechanisms involved in the recognition of unfolded transmembrane proteins. One system uses chaperones to detect unfolded cytoplasmic domains of transmembrane proteins, whereas the second mechanism relies on an internal quality control system of the protein, which can trigger degradation when the protein deviates from the folded state. Both quality control mechanisms are key to prevent proteotoxic effects at the cell surface and to ensure cell integrity. |
format | Online Article Text |
id | pubmed-3987138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39871382014-10-14 Quality control at the plasma membrane: One mechanism does not fit all Babst, Markus J Cell Biol Reviews The plasma membrane quality control system of eukaryotic cells is able to recognize and degrade damaged cell surface proteins. Recent studies have identified two mechanisms involved in the recognition of unfolded transmembrane proteins. One system uses chaperones to detect unfolded cytoplasmic domains of transmembrane proteins, whereas the second mechanism relies on an internal quality control system of the protein, which can trigger degradation when the protein deviates from the folded state. Both quality control mechanisms are key to prevent proteotoxic effects at the cell surface and to ensure cell integrity. The Rockefeller University Press 2014-04-14 /pmc/articles/PMC3987138/ /pubmed/24733583 http://dx.doi.org/10.1083/jcb.201310113 Text en © 2014 Babst 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 Babst, Markus Quality control at the plasma membrane: One mechanism does not fit all |
title | Quality control at the plasma membrane: One mechanism does not fit all |
title_full | Quality control at the plasma membrane: One mechanism does not fit all |
title_fullStr | Quality control at the plasma membrane: One mechanism does not fit all |
title_full_unstemmed | Quality control at the plasma membrane: One mechanism does not fit all |
title_short | Quality control at the plasma membrane: One mechanism does not fit all |
title_sort | quality control at the plasma membrane: one mechanism does not fit all |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987138/ https://www.ncbi.nlm.nih.gov/pubmed/24733583 http://dx.doi.org/10.1083/jcb.201310113 |
work_keys_str_mv | AT babstmarkus qualitycontrolattheplasmamembraneonemechanismdoesnotfitall |