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A snapshot of protein trafficking in SARS‐CoV‐2 infection

SARS‐CoV‐2 is a human pathogenic virus responsible for the COVID‐19 (coronavirus disease 2019) pandemic. The infection cycle of SARS‐CoV‐2 involves several related steps, including virus entry, gene expression, RNA replication, assembly of infectious virions and their egress. For all of these steps,...

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Detalles Bibliográficos
Autores principales: Prasad, Vibhu, Bartenschlager, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874443/
https://www.ncbi.nlm.nih.gov/pubmed/36314261
http://dx.doi.org/10.1111/boc.202200073
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author Prasad, Vibhu
Bartenschlager, Ralf
author_facet Prasad, Vibhu
Bartenschlager, Ralf
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description SARS‐CoV‐2 is a human pathogenic virus responsible for the COVID‐19 (coronavirus disease 2019) pandemic. The infection cycle of SARS‐CoV‐2 involves several related steps, including virus entry, gene expression, RNA replication, assembly of infectious virions and their egress. For all of these steps, the virus relies on and exploits host cell factors, cellular organelles, and processes such as endocytosis, nuclear transport, protein secretion, metabolite transport at membrane contact sites (MSC) and exocytotic pathways. To do this, SARS‐CoV‐2 has evolved multifunctional viral proteins that hijack cellular factors and modulate their function by unique strategies. In this Review, we highlight cellular trafficking factors, processes, and organelles of relevance to the SARS‐CoV‐2 infection cycle and how viral proteins make use of and perturb cellular transport during the viral infection cycle.
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spelling pubmed-98744432023-01-25 A snapshot of protein trafficking in SARS‐CoV‐2 infection Prasad, Vibhu Bartenschlager, Ralf Biol Cell Review SARS‐CoV‐2 is a human pathogenic virus responsible for the COVID‐19 (coronavirus disease 2019) pandemic. The infection cycle of SARS‐CoV‐2 involves several related steps, including virus entry, gene expression, RNA replication, assembly of infectious virions and their egress. For all of these steps, the virus relies on and exploits host cell factors, cellular organelles, and processes such as endocytosis, nuclear transport, protein secretion, metabolite transport at membrane contact sites (MSC) and exocytotic pathways. To do this, SARS‐CoV‐2 has evolved multifunctional viral proteins that hijack cellular factors and modulate their function by unique strategies. In this Review, we highlight cellular trafficking factors, processes, and organelles of relevance to the SARS‐CoV‐2 infection cycle and how viral proteins make use of and perturb cellular transport during the viral infection cycle. John Wiley and Sons Inc. 2022-11-14 /pmc/articles/PMC9874443/ /pubmed/36314261 http://dx.doi.org/10.1111/boc.202200073 Text en © 2021 The Authors. Biology of the Cell published by Wiley‐VCH GmbH on behalf of Société Française des Microscopies and Société de Biologie Cellulaire de France https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review
Prasad, Vibhu
Bartenschlager, Ralf
A snapshot of protein trafficking in SARS‐CoV‐2 infection
title A snapshot of protein trafficking in SARS‐CoV‐2 infection
title_full A snapshot of protein trafficking in SARS‐CoV‐2 infection
title_fullStr A snapshot of protein trafficking in SARS‐CoV‐2 infection
title_full_unstemmed A snapshot of protein trafficking in SARS‐CoV‐2 infection
title_short A snapshot of protein trafficking in SARS‐CoV‐2 infection
title_sort snapshot of protein trafficking in sars‐cov‐2 infection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874443/
https://www.ncbi.nlm.nih.gov/pubmed/36314261
http://dx.doi.org/10.1111/boc.202200073
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