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SARS-CoV-2 S glycoprotein binding to multiple host receptors enables cell entry and infection
The severe acute respiratory syndrome-related coronavirus-2 (SARS-CoV-2) infection displays a wide array of clinical manifestations. Although some risk factors for coronavirus disease 2019 (COVID-19) severity and outcomes have been identified the underlying biologic mechanisms are still not well und...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450557/ https://www.ncbi.nlm.nih.gov/pubmed/34542788 http://dx.doi.org/10.1007/s10719-021-10021-z |
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author | Trbojević-Akmačić, Irena Petrović, Tea Lauc, Gordan |
author_facet | Trbojević-Akmačić, Irena Petrović, Tea Lauc, Gordan |
author_sort | Trbojević-Akmačić, Irena |
collection | PubMed |
description | The severe acute respiratory syndrome-related coronavirus-2 (SARS-CoV-2) infection displays a wide array of clinical manifestations. Although some risk factors for coronavirus disease 2019 (COVID-19) severity and outcomes have been identified the underlying biologic mechanisms are still not well understood. The surface SARS-CoV-2 proteins are heavily glycosylated enabling host cell interaction and viral entry. Angiotensin-converting enzyme 2 (ACE2) has been identified to be the main host cell receptor enabling SARS-CoV-2 cell entry after interaction with its S glycoprotein. However, recent studies report SARS-CoV-2 S glycoprotein interaction with other cell receptors, mainly C-type lectins which recognize specific glycan epitopes facilitating SARS-CoV-2 entry to susceptible cells. Here, we are summarizing the main findings on SARS-CoV-2 interactions with ACE2 and other cell membrane surface receptors and soluble lectins involved in the viral cell entry modulating its infectivity and potentially playing a role in subsequent clinical manifestations of COVID-19. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-8450557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-84505572021-09-20 SARS-CoV-2 S glycoprotein binding to multiple host receptors enables cell entry and infection Trbojević-Akmačić, Irena Petrović, Tea Lauc, Gordan Glycoconj J Mini Review The severe acute respiratory syndrome-related coronavirus-2 (SARS-CoV-2) infection displays a wide array of clinical manifestations. Although some risk factors for coronavirus disease 2019 (COVID-19) severity and outcomes have been identified the underlying biologic mechanisms are still not well understood. The surface SARS-CoV-2 proteins are heavily glycosylated enabling host cell interaction and viral entry. Angiotensin-converting enzyme 2 (ACE2) has been identified to be the main host cell receptor enabling SARS-CoV-2 cell entry after interaction with its S glycoprotein. However, recent studies report SARS-CoV-2 S glycoprotein interaction with other cell receptors, mainly C-type lectins which recognize specific glycan epitopes facilitating SARS-CoV-2 entry to susceptible cells. Here, we are summarizing the main findings on SARS-CoV-2 interactions with ACE2 and other cell membrane surface receptors and soluble lectins involved in the viral cell entry modulating its infectivity and potentially playing a role in subsequent clinical manifestations of COVID-19. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2021-09-20 2021 /pmc/articles/PMC8450557/ /pubmed/34542788 http://dx.doi.org/10.1007/s10719-021-10021-z Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Mini Review Trbojević-Akmačić, Irena Petrović, Tea Lauc, Gordan SARS-CoV-2 S glycoprotein binding to multiple host receptors enables cell entry and infection |
title | SARS-CoV-2 S glycoprotein binding to multiple host receptors enables cell entry and infection |
title_full | SARS-CoV-2 S glycoprotein binding to multiple host receptors enables cell entry and infection |
title_fullStr | SARS-CoV-2 S glycoprotein binding to multiple host receptors enables cell entry and infection |
title_full_unstemmed | SARS-CoV-2 S glycoprotein binding to multiple host receptors enables cell entry and infection |
title_short | SARS-CoV-2 S glycoprotein binding to multiple host receptors enables cell entry and infection |
title_sort | sars-cov-2 s glycoprotein binding to multiple host receptors enables cell entry and infection |
topic | Mini Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450557/ https://www.ncbi.nlm.nih.gov/pubmed/34542788 http://dx.doi.org/10.1007/s10719-021-10021-z |
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