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A Collection of Designed Peptides to Target SARS-CoV-2 Spike RBD—ACE2 Interaction
The angiotensin-converting enzyme 2 (ACE2) is the receptor used by SARS-CoV and SARS-CoV-2 coronaviruses to attach to cells via the receptor-binding domain (RBD) of their viral spike protein. Since the start of the COVID-19 pandemic, several structures of protein complexes involving ACE2 and RBD as...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584250/ https://www.ncbi.nlm.nih.gov/pubmed/34769056 http://dx.doi.org/10.3390/ijms222111627 |
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author | Fernandez-Fuentes, Narcis Molina, Ruben Oliva, Baldo |
author_facet | Fernandez-Fuentes, Narcis Molina, Ruben Oliva, Baldo |
author_sort | Fernandez-Fuentes, Narcis |
collection | PubMed |
description | The angiotensin-converting enzyme 2 (ACE2) is the receptor used by SARS-CoV and SARS-CoV-2 coronaviruses to attach to cells via the receptor-binding domain (RBD) of their viral spike protein. Since the start of the COVID-19 pandemic, several structures of protein complexes involving ACE2 and RBD as well as monoclonal antibodies and nanobodies have become available. We have leveraged the structural data to design peptides to target the interaction between the RBD of SARS-CoV-2 and ACE2 and SARS-CoV and ACE2, as contrasting exemplar, as well as the dimerization surface of ACE2 monomers. The peptides were modelled using our original method: PiPreD that uses native elements of the interaction between the targeted protein and cognate partner(s) that are subsequently included in the designed peptides. These peptides recapitulate stretches of residues present in the native interface plus novel and highly diverse conformations surrogating key interactions at the interface. To facilitate the access to this information we have created a freely available and dedicated web-based repository, PepI-Covid19 database, providing convenient access to this wealth of information to the scientific community with the view of maximizing its potential impact in the development of novel therapeutic and diagnostic agents. |
format | Online Article Text |
id | pubmed-8584250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85842502021-11-12 A Collection of Designed Peptides to Target SARS-CoV-2 Spike RBD—ACE2 Interaction Fernandez-Fuentes, Narcis Molina, Ruben Oliva, Baldo Int J Mol Sci Article The angiotensin-converting enzyme 2 (ACE2) is the receptor used by SARS-CoV and SARS-CoV-2 coronaviruses to attach to cells via the receptor-binding domain (RBD) of their viral spike protein. Since the start of the COVID-19 pandemic, several structures of protein complexes involving ACE2 and RBD as well as monoclonal antibodies and nanobodies have become available. We have leveraged the structural data to design peptides to target the interaction between the RBD of SARS-CoV-2 and ACE2 and SARS-CoV and ACE2, as contrasting exemplar, as well as the dimerization surface of ACE2 monomers. The peptides were modelled using our original method: PiPreD that uses native elements of the interaction between the targeted protein and cognate partner(s) that are subsequently included in the designed peptides. These peptides recapitulate stretches of residues present in the native interface plus novel and highly diverse conformations surrogating key interactions at the interface. To facilitate the access to this information we have created a freely available and dedicated web-based repository, PepI-Covid19 database, providing convenient access to this wealth of information to the scientific community with the view of maximizing its potential impact in the development of novel therapeutic and diagnostic agents. MDPI 2021-10-27 /pmc/articles/PMC8584250/ /pubmed/34769056 http://dx.doi.org/10.3390/ijms222111627 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fernandez-Fuentes, Narcis Molina, Ruben Oliva, Baldo A Collection of Designed Peptides to Target SARS-CoV-2 Spike RBD—ACE2 Interaction |
title | A Collection of Designed Peptides to Target SARS-CoV-2 Spike RBD—ACE2 Interaction |
title_full | A Collection of Designed Peptides to Target SARS-CoV-2 Spike RBD—ACE2 Interaction |
title_fullStr | A Collection of Designed Peptides to Target SARS-CoV-2 Spike RBD—ACE2 Interaction |
title_full_unstemmed | A Collection of Designed Peptides to Target SARS-CoV-2 Spike RBD—ACE2 Interaction |
title_short | A Collection of Designed Peptides to Target SARS-CoV-2 Spike RBD—ACE2 Interaction |
title_sort | collection of designed peptides to target sars-cov-2 spike rbd—ace2 interaction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584250/ https://www.ncbi.nlm.nih.gov/pubmed/34769056 http://dx.doi.org/10.3390/ijms222111627 |
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