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Membrane rearrangements mediated by coronavirus nonstructural proteins 3 and 4
Coronaviruses replicate their genomes in association with rearranged cellular membranes. The coronavirus nonstructural integral membrane proteins (nsps) 3, 4 and 6, are key players in the formation of the rearranged membranes. Previously, we demonstrated that nsp3 and nsp4 interact and that their co...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111329/ https://www.ncbi.nlm.nih.gov/pubmed/24928045 http://dx.doi.org/10.1016/j.virol.2014.04.027 |
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author | Hagemeijer, Marne C. Monastyrska, Iryna Griffith, Janice van der Sluijs, Peter Voortman, Jarno van Bergen en Henegouwen, Paul M. Vonk, Annelotte M. Rottier, Peter J.M. Reggiori, Fulvio de Haan, Cornelis A.M. |
author_facet | Hagemeijer, Marne C. Monastyrska, Iryna Griffith, Janice van der Sluijs, Peter Voortman, Jarno van Bergen en Henegouwen, Paul M. Vonk, Annelotte M. Rottier, Peter J.M. Reggiori, Fulvio de Haan, Cornelis A.M. |
author_sort | Hagemeijer, Marne C. |
collection | PubMed |
description | Coronaviruses replicate their genomes in association with rearranged cellular membranes. The coronavirus nonstructural integral membrane proteins (nsps) 3, 4 and 6, are key players in the formation of the rearranged membranes. Previously, we demonstrated that nsp3 and nsp4 interact and that their co-expression results in the relocalization of these proteins from the endoplasmic reticulum (ER) into discrete perinuclear foci. We now show that these foci correspond to areas of rearranged ER-derived membranes, which display increased membrane curvature. These structures, which were able to recruit other nsps, were only detected when nsp3 and nsp4 were derived from the same coronavirus species. We propose, based on the analysis of a large number of nsp3 and nsp4 mutants, that interaction between the large luminal loops of these proteins drives the formation of membrane rearrangements, onto which the coronavirus replication–transcription complexes assemble in infected cells. |
format | Online Article Text |
id | pubmed-7111329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71113292020-04-02 Membrane rearrangements mediated by coronavirus nonstructural proteins 3 and 4 Hagemeijer, Marne C. Monastyrska, Iryna Griffith, Janice van der Sluijs, Peter Voortman, Jarno van Bergen en Henegouwen, Paul M. Vonk, Annelotte M. Rottier, Peter J.M. Reggiori, Fulvio de Haan, Cornelis A.M. Virology Article Coronaviruses replicate their genomes in association with rearranged cellular membranes. The coronavirus nonstructural integral membrane proteins (nsps) 3, 4 and 6, are key players in the formation of the rearranged membranes. Previously, we demonstrated that nsp3 and nsp4 interact and that their co-expression results in the relocalization of these proteins from the endoplasmic reticulum (ER) into discrete perinuclear foci. We now show that these foci correspond to areas of rearranged ER-derived membranes, which display increased membrane curvature. These structures, which were able to recruit other nsps, were only detected when nsp3 and nsp4 were derived from the same coronavirus species. We propose, based on the analysis of a large number of nsp3 and nsp4 mutants, that interaction between the large luminal loops of these proteins drives the formation of membrane rearrangements, onto which the coronavirus replication–transcription complexes assemble in infected cells. Elsevier Inc. 2014-06 2014-05-13 /pmc/articles/PMC7111329/ /pubmed/24928045 http://dx.doi.org/10.1016/j.virol.2014.04.027 Text en Copyright © 2014 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Hagemeijer, Marne C. Monastyrska, Iryna Griffith, Janice van der Sluijs, Peter Voortman, Jarno van Bergen en Henegouwen, Paul M. Vonk, Annelotte M. Rottier, Peter J.M. Reggiori, Fulvio de Haan, Cornelis A.M. Membrane rearrangements mediated by coronavirus nonstructural proteins 3 and 4 |
title | Membrane rearrangements mediated by coronavirus nonstructural proteins 3 and 4 |
title_full | Membrane rearrangements mediated by coronavirus nonstructural proteins 3 and 4 |
title_fullStr | Membrane rearrangements mediated by coronavirus nonstructural proteins 3 and 4 |
title_full_unstemmed | Membrane rearrangements mediated by coronavirus nonstructural proteins 3 and 4 |
title_short | Membrane rearrangements mediated by coronavirus nonstructural proteins 3 and 4 |
title_sort | membrane rearrangements mediated by coronavirus nonstructural proteins 3 and 4 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111329/ https://www.ncbi.nlm.nih.gov/pubmed/24928045 http://dx.doi.org/10.1016/j.virol.2014.04.027 |
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