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Targeting neuropilins as a viable SARS‐CoV‐2 treatment

The SARS‐CoV‐2 pandemic has significantly impacted global health. Research on viral mechanisms, highly effective vaccines, and other therapies is in progress. Neuropilins have recently been identified as host cell receptors enabling viral fusion. Here, we provide context to neuropilin's tissue‐...

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Detalles Bibliográficos
Autores principales: Sarabipour, Sarvenaz, Mac Gabhann, Feilim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8420456/
https://www.ncbi.nlm.nih.gov/pubmed/34185437
http://dx.doi.org/10.1111/febs.16096
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author Sarabipour, Sarvenaz
Mac Gabhann, Feilim
author_facet Sarabipour, Sarvenaz
Mac Gabhann, Feilim
author_sort Sarabipour, Sarvenaz
collection PubMed
description The SARS‐CoV‐2 pandemic has significantly impacted global health. Research on viral mechanisms, highly effective vaccines, and other therapies is in progress. Neuropilins have recently been identified as host cell receptors enabling viral fusion. Here, we provide context to neuropilin's tissue‐specific role in infection and the potential impact of NRP‐based therapeutics. We conclude that the central roles of neuropilins in vascular, neural, and other pathways may render it a less suitable target for treating SARS‐CoV‐2 than agents that target its binding partner, the viral spike protein.
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spelling pubmed-84204562021-09-07 Targeting neuropilins as a viable SARS‐CoV‐2 treatment Sarabipour, Sarvenaz Mac Gabhann, Feilim FEBS J Viewpoint The SARS‐CoV‐2 pandemic has significantly impacted global health. Research on viral mechanisms, highly effective vaccines, and other therapies is in progress. Neuropilins have recently been identified as host cell receptors enabling viral fusion. Here, we provide context to neuropilin's tissue‐specific role in infection and the potential impact of NRP‐based therapeutics. We conclude that the central roles of neuropilins in vascular, neural, and other pathways may render it a less suitable target for treating SARS‐CoV‐2 than agents that target its binding partner, the viral spike protein. John Wiley and Sons Inc. 2021-07-12 2021-09 /pmc/articles/PMC8420456/ /pubmed/34185437 http://dx.doi.org/10.1111/febs.16096 Text en © 2021 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies 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 Viewpoint
Sarabipour, Sarvenaz
Mac Gabhann, Feilim
Targeting neuropilins as a viable SARS‐CoV‐2 treatment
title Targeting neuropilins as a viable SARS‐CoV‐2 treatment
title_full Targeting neuropilins as a viable SARS‐CoV‐2 treatment
title_fullStr Targeting neuropilins as a viable SARS‐CoV‐2 treatment
title_full_unstemmed Targeting neuropilins as a viable SARS‐CoV‐2 treatment
title_short Targeting neuropilins as a viable SARS‐CoV‐2 treatment
title_sort targeting neuropilins as a viable sars‐cov‐2 treatment
topic Viewpoint
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8420456/
https://www.ncbi.nlm.nih.gov/pubmed/34185437
http://dx.doi.org/10.1111/febs.16096
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