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Human coronavirus spike protein-host receptor recognition

A variety of coronaviruses (CoVs) have infected humans and caused mild to severe respiratory diseases that could result in mortality. The human CoVs (HCoVs) belong to the genera of α- and β-CoVs that originate in rodents and bats and are transmitted to humans via zoonotic contacts. The binding of vi...

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Autor principal: Guruprasad, Lalitha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7604128/
https://www.ncbi.nlm.nih.gov/pubmed/33137344
http://dx.doi.org/10.1016/j.pbiomolbio.2020.10.006
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author Guruprasad, Lalitha
author_facet Guruprasad, Lalitha
author_sort Guruprasad, Lalitha
collection PubMed
description A variety of coronaviruses (CoVs) have infected humans and caused mild to severe respiratory diseases that could result in mortality. The human CoVs (HCoVs) belong to the genera of α- and β-CoVs that originate in rodents and bats and are transmitted to humans via zoonotic contacts. The binding of viral spike proteins to the host cell receptors is essential for mediating fusion of viral and host cell membranes to cause infection. The SARS-CoV-2 originated in bats (RaTG13 SARS-CoV) and is transmitted to humans via pangolins. The presence of 'PRRA' sequence motif in SARS-CoV-2 spike proteins from human, dog, cat, mink, tiger and lion suggests a common viral entry mechanism into host cells. In this review, we discuss structural features of HCoV spike proteins and recognition of host protein and carbohydrate receptors.
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spelling pubmed-76041282020-11-02 Human coronavirus spike protein-host receptor recognition Guruprasad, Lalitha Prog Biophys Mol Biol Article A variety of coronaviruses (CoVs) have infected humans and caused mild to severe respiratory diseases that could result in mortality. The human CoVs (HCoVs) belong to the genera of α- and β-CoVs that originate in rodents and bats and are transmitted to humans via zoonotic contacts. The binding of viral spike proteins to the host cell receptors is essential for mediating fusion of viral and host cell membranes to cause infection. The SARS-CoV-2 originated in bats (RaTG13 SARS-CoV) and is transmitted to humans via pangolins. The presence of 'PRRA' sequence motif in SARS-CoV-2 spike proteins from human, dog, cat, mink, tiger and lion suggests a common viral entry mechanism into host cells. In this review, we discuss structural features of HCoV spike proteins and recognition of host protein and carbohydrate receptors. Elsevier Ltd. 2021-05 2020-10-31 /pmc/articles/PMC7604128/ /pubmed/33137344 http://dx.doi.org/10.1016/j.pbiomolbio.2020.10.006 Text en © 2020 Elsevier Ltd. 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
Guruprasad, Lalitha
Human coronavirus spike protein-host receptor recognition
title Human coronavirus spike protein-host receptor recognition
title_full Human coronavirus spike protein-host receptor recognition
title_fullStr Human coronavirus spike protein-host receptor recognition
title_full_unstemmed Human coronavirus spike protein-host receptor recognition
title_short Human coronavirus spike protein-host receptor recognition
title_sort human coronavirus spike protein-host receptor recognition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7604128/
https://www.ncbi.nlm.nih.gov/pubmed/33137344
http://dx.doi.org/10.1016/j.pbiomolbio.2020.10.006
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