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Peptide Platform as a Powerful Tool in the Fight against COVID-19.
- Source :
-
Viruses [Viruses] 2021 Aug 23; Vol. 13 (8). Date of Electronic Publication: 2021 Aug 23. - Publication Year :
- 2021
-
Abstract
- 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.
- Subjects :
- Angiotensin-Converting Enzyme 2 chemistry
Angiotensin-Converting Enzyme 2 metabolism
Animals
Antibodies, Neutralizing immunology
Antibodies, Viral immunology
Broadly Neutralizing Antibodies immunology
COVID-19 prevention & control
COVID-19 Vaccines immunology
Chlorocebus aethiops
Dipeptidyl Peptidase 4 metabolism
Epitopes, T-Lymphocyte immunology
Humans
Mice
Mice, Inbred BALB C
Models, Molecular
Molecular Docking Simulation
Molecular Dynamics Simulation
Peptide Fragments chemistry
Peptide Fragments metabolism
Protein Binding
Protein Domains
Receptors, Coronavirus chemistry
Receptors, Coronavirus metabolism
SARS-CoV-2 chemistry
SARS-CoV-2 physiology
Spike Glycoprotein, Coronavirus chemistry
Spike Glycoprotein, Coronavirus metabolism
Vero Cells
Virus Internalization
COVID-19 Drug Treatment
Dipeptidyl Peptidase 4 chemistry
Peptide Fragments immunology
Peptide Fragments pharmacology
SARS-CoV-2 drug effects
SARS-CoV-2 immunology
Spike Glycoprotein, Coronavirus immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1999-4915
- Volume :
- 13
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Viruses
- Publication Type :
- Academic Journal
- Accession number :
- 34452531
- Full Text :
- https://doi.org/10.3390/v13081667