Data di Pubblicazione:
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.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
COVID-19; peptides; protein-protein docking; conserved RBD region; SARS-CoV-2 variants; VSVpp.SARS-2S; drug design
Elenco autori:
Rossi, Antonio
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