Viruses · 2021
Peptide Platform as a Powerful Tool in the Fight against COVID-19.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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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
Аннотация
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.
Предметные рубрики MeSH
Angiotensin-Converting Enzyme 2AnimalsAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesCOVID-19COVID-19 VaccinesChlorocebus aethiopsDipeptidyl Peptidase 4Epitopes, T-LymphocyteHumansMiceMice, Inbred BALB CModels, MolecularMolecular Docking SimulationMolecular Dynamics SimulationPeptide FragmentsProtein BindingProtein DomainsReceptors, CoronavirusSARS-CoV-2Spike Glycoprotein, CoronavirusVero CellsVirus InternalizationCOVID-19 Drug Treatment