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Peptide and peptide-based inhibitors of SARS-CoV-2 entry

To date, no effective vaccines or therapies are available against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative pandemic agent of the coronavirus disease 2019 (COVID-19). Due to their safety, efficacy and specificity, peptide inhibitors hold great promise for the tr...

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Autores principales: Schütz, Desiree, Ruiz-Blanco, Yasser B., Münch, Jan, Kirchhoff, Frank, Sanchez-Garcia, Elsa, Müller, Janis A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). Published by Elsevier B.V. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7665879/
https://www.ncbi.nlm.nih.gov/pubmed/33189768
http://dx.doi.org/10.1016/j.addr.2020.11.007
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author Schütz, Desiree
Ruiz-Blanco, Yasser B.
Münch, Jan
Kirchhoff, Frank
Sanchez-Garcia, Elsa
Müller, Janis A.
author_facet Schütz, Desiree
Ruiz-Blanco, Yasser B.
Münch, Jan
Kirchhoff, Frank
Sanchez-Garcia, Elsa
Müller, Janis A.
author_sort Schütz, Desiree
collection PubMed
description To date, no effective vaccines or therapies are available against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative pandemic agent of the coronavirus disease 2019 (COVID-19). Due to their safety, efficacy and specificity, peptide inhibitors hold great promise for the treatment of newly emerging viral pathogens. Based on the known structures of viral proteins and their cellular targets, antiviral peptides can be rationally designed and optimized. The resulting peptides may be highly specific for their respective targets and particular viral pathogens or exert broad antiviral activity. Here, we summarize the current status of peptides inhibiting SARS-CoV-2 entry and outline the strategies used to design peptides targeting the ACE2 receptor or the viral spike protein and its activating proteases furin, transmembrane serine protease 2 (TMPRSS2), or cathepsin L. In addition, we present approaches used against related viruses such as SARS-CoV-1 that might be implemented for inhibition of SARS-CoV-2 infection.
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spelling pubmed-76658792020-11-16 Peptide and peptide-based inhibitors of SARS-CoV-2 entry Schütz, Desiree Ruiz-Blanco, Yasser B. Münch, Jan Kirchhoff, Frank Sanchez-Garcia, Elsa Müller, Janis A. Adv Drug Deliv Rev Article To date, no effective vaccines or therapies are available against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative pandemic agent of the coronavirus disease 2019 (COVID-19). Due to their safety, efficacy and specificity, peptide inhibitors hold great promise for the treatment of newly emerging viral pathogens. Based on the known structures of viral proteins and their cellular targets, antiviral peptides can be rationally designed and optimized. The resulting peptides may be highly specific for their respective targets and particular viral pathogens or exert broad antiviral activity. Here, we summarize the current status of peptides inhibiting SARS-CoV-2 entry and outline the strategies used to design peptides targeting the ACE2 receptor or the viral spike protein and its activating proteases furin, transmembrane serine protease 2 (TMPRSS2), or cathepsin L. In addition, we present approaches used against related viruses such as SARS-CoV-1 that might be implemented for inhibition of SARS-CoV-2 infection. The Author(s). Published by Elsevier B.V. 2020-12 2020-11-13 /pmc/articles/PMC7665879/ /pubmed/33189768 http://dx.doi.org/10.1016/j.addr.2020.11.007 Text en © 2020 The Authors 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
Schütz, Desiree
Ruiz-Blanco, Yasser B.
Münch, Jan
Kirchhoff, Frank
Sanchez-Garcia, Elsa
Müller, Janis A.
Peptide and peptide-based inhibitors of SARS-CoV-2 entry
title Peptide and peptide-based inhibitors of SARS-CoV-2 entry
title_full Peptide and peptide-based inhibitors of SARS-CoV-2 entry
title_fullStr Peptide and peptide-based inhibitors of SARS-CoV-2 entry
title_full_unstemmed Peptide and peptide-based inhibitors of SARS-CoV-2 entry
title_short Peptide and peptide-based inhibitors of SARS-CoV-2 entry
title_sort peptide and peptide-based inhibitors of sars-cov-2 entry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7665879/
https://www.ncbi.nlm.nih.gov/pubmed/33189768
http://dx.doi.org/10.1016/j.addr.2020.11.007
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