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Targeting the SARS-CoV-2-spike protein: from antibodies to miniproteins and peptides

Coronavirus disease-19, caused by the novel β-coronavirus SARS-CoV-2, has created a global pandemic unseen in a century. Rapid worldwide efforts have enabled the characterization of the virus and its pathogenic mechanism. An early key finding is that SARS-CoV-2 uses spike proteins, the virus' m...

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Autor principal: Pomplun, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128053/
https://www.ncbi.nlm.nih.gov/pubmed/34041482
http://dx.doi.org/10.1039/d0md00385a
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author Pomplun, Sebastian
author_facet Pomplun, Sebastian
author_sort Pomplun, Sebastian
collection PubMed
description Coronavirus disease-19, caused by the novel β-coronavirus SARS-CoV-2, has created a global pandemic unseen in a century. Rapid worldwide efforts have enabled the characterization of the virus and its pathogenic mechanism. An early key finding is that SARS-CoV-2 uses spike proteins, the virus' most exposed structures, to bind to human ACE2 receptors and initiate cell invasion. Competitive targeting of the spike protein is a promising strategy to neutralize virus infectivity. This review article summarizes the discovery, binding modes and eventual applications of several classes of (bio)molecules targeting the spike protein: antibodies, nanobodies, soluble ACE2 variants, miniproteins, peptides and small molecules.
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spelling pubmed-81280532021-05-25 Targeting the SARS-CoV-2-spike protein: from antibodies to miniproteins and peptides Pomplun, Sebastian RSC Med Chem Chemistry Coronavirus disease-19, caused by the novel β-coronavirus SARS-CoV-2, has created a global pandemic unseen in a century. Rapid worldwide efforts have enabled the characterization of the virus and its pathogenic mechanism. An early key finding is that SARS-CoV-2 uses spike proteins, the virus' most exposed structures, to bind to human ACE2 receptors and initiate cell invasion. Competitive targeting of the spike protein is a promising strategy to neutralize virus infectivity. This review article summarizes the discovery, binding modes and eventual applications of several classes of (bio)molecules targeting the spike protein: antibodies, nanobodies, soluble ACE2 variants, miniproteins, peptides and small molecules. RSC 2020-12-17 /pmc/articles/PMC8128053/ /pubmed/34041482 http://dx.doi.org/10.1039/d0md00385a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Pomplun, Sebastian
Targeting the SARS-CoV-2-spike protein: from antibodies to miniproteins and peptides
title Targeting the SARS-CoV-2-spike protein: from antibodies to miniproteins and peptides
title_full Targeting the SARS-CoV-2-spike protein: from antibodies to miniproteins and peptides
title_fullStr Targeting the SARS-CoV-2-spike protein: from antibodies to miniproteins and peptides
title_full_unstemmed Targeting the SARS-CoV-2-spike protein: from antibodies to miniproteins and peptides
title_short Targeting the SARS-CoV-2-spike protein: from antibodies to miniproteins and peptides
title_sort targeting the sars-cov-2-spike protein: from antibodies to miniproteins and peptides
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128053/
https://www.ncbi.nlm.nih.gov/pubmed/34041482
http://dx.doi.org/10.1039/d0md00385a
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