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Peptide Platform as a Powerful Tool in the Fight against COVID-19
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in a global pandemic causing over 195 million infections and more than 4 million fatalities as of July 2021.To date, it has been demonstrated that a number of mutations in the spike glycoprotein (S protein) of SARS-CoV-2 varia...
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/PMC8402770/ https://www.ncbi.nlm.nih.gov/pubmed/34452531 http://dx.doi.org/10.3390/v13081667 |
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author | Murdocca, Michela Citro, Gennaro Romeo, Isabella Lupia, Antonio Miersch, Shane Amadio, Bruno Bonomo, Alessia Rossi, Antonio Sidhu, Sachdev S. Pandolfi, Pier Paolo Alcaro, Stefano Sangiuolo, Federica Carla Novelli, Giuseppe |
author_facet | Murdocca, Michela Citro, Gennaro Romeo, Isabella Lupia, Antonio Miersch, Shane Amadio, Bruno Bonomo, Alessia Rossi, Antonio Sidhu, Sachdev S. Pandolfi, Pier Paolo Alcaro, Stefano Sangiuolo, Federica Carla Novelli, Giuseppe |
author_sort | Murdocca, Michela |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in a global pandemic causing over 195 million infections and more than 4 million fatalities as of July 2021.To date, it has been demonstrated that a number of mutations in the spike glycoprotein (S protein) of SARS-CoV-2 variants of concern abrogate or reduce the neutralization potency of several therapeutic antibodies and vaccine-elicited antibodies. Therefore, the development of additional vaccine platforms with improved supply and logistic profile remains a pressing need. In this work, we have validated the applicability of a peptide-based strategy focused on a preventive as well as a therapeutic purpose. On the basis of the involvement of the dipeptidyl peptidase 4 (DPP4), in addition to the angiotensin converting enzyme 2 (ACE2) receptor in the mechanism of virus entry, we analyzed peptides bearing DPP4 sequences by protein–protein docking and assessed their ability to block pseudovirus infection in vitro. In parallel, we have selected and synthetized peptide sequences located within the highly conserved receptor-binding domain (RBD) of the S protein, and we found that RBD-based vaccines could better promote elicitation of high titers of neutralizing antibodies specific against the regions of interest, as confirmed by immunoinformatic methodologies and in vivo studies. These findings unveil a key antigenic site targeted by broadly neutralizing antibodies and pave the way to the design of pan-coronavirus vaccines. |
format | Online Article Text |
id | pubmed-8402770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84027702021-08-29 Peptide Platform as a Powerful Tool in the Fight against COVID-19 Murdocca, Michela Citro, Gennaro Romeo, Isabella Lupia, Antonio Miersch, Shane Amadio, Bruno Bonomo, Alessia Rossi, Antonio Sidhu, Sachdev S. Pandolfi, Pier Paolo Alcaro, Stefano Sangiuolo, Federica Carla Novelli, Giuseppe Viruses Article Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in a global pandemic causing over 195 million infections and more than 4 million fatalities as of July 2021.To date, it has been demonstrated that a number of mutations in the spike glycoprotein (S protein) of SARS-CoV-2 variants of concern abrogate or reduce the neutralization potency of several therapeutic antibodies and vaccine-elicited antibodies. Therefore, the development of additional vaccine platforms with improved supply and logistic profile remains a pressing need. In this work, we have validated the applicability of a peptide-based strategy focused on a preventive as well as a therapeutic purpose. On the basis of the involvement of the dipeptidyl peptidase 4 (DPP4), in addition to the angiotensin converting enzyme 2 (ACE2) receptor in the mechanism of virus entry, we analyzed peptides bearing DPP4 sequences by protein–protein docking and assessed their ability to block pseudovirus infection in vitro. In parallel, we have selected and synthetized peptide sequences located within the highly conserved receptor-binding domain (RBD) of the S protein, and we found that RBD-based vaccines could better promote elicitation of high titers of neutralizing antibodies specific against the regions of interest, as confirmed by immunoinformatic methodologies and in vivo studies. These findings unveil a key antigenic site targeted by broadly neutralizing antibodies and pave the way to the design of pan-coronavirus vaccines. MDPI 2021-08-23 /pmc/articles/PMC8402770/ /pubmed/34452531 http://dx.doi.org/10.3390/v13081667 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 Murdocca, Michela Citro, Gennaro Romeo, Isabella Lupia, Antonio Miersch, Shane Amadio, Bruno Bonomo, Alessia Rossi, Antonio Sidhu, Sachdev S. Pandolfi, Pier Paolo Alcaro, Stefano Sangiuolo, Federica Carla Novelli, Giuseppe Peptide Platform as a Powerful Tool in the Fight against COVID-19 |
title | Peptide Platform as a Powerful Tool in the Fight against COVID-19 |
title_full | Peptide Platform as a Powerful Tool in the Fight against COVID-19 |
title_fullStr | Peptide Platform as a Powerful Tool in the Fight against COVID-19 |
title_full_unstemmed | Peptide Platform as a Powerful Tool in the Fight against COVID-19 |
title_short | Peptide Platform as a Powerful Tool in the Fight against COVID-19 |
title_sort | peptide platform as a powerful tool in the fight against covid-19 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402770/ https://www.ncbi.nlm.nih.gov/pubmed/34452531 http://dx.doi.org/10.3390/v13081667 |
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