| Literature DB >> 33580154 |
Philippe Karoyan1,2,3, Vincent Vieillard4, Luis Gómez-Morales5,6, Estelle Odile5,6, Amélie Guihot7,8, Charles-Edouard Luyt9, Alexis Denis10, Pascal Grondin10, Olivier Lequin5.
Abstract
In light of the recent accumulated knowledge on SARS-CoV-2 and its mode of human cells invasion, the binding of viral spike glycoprotein to human Angiotensin Converting Enzyme 2 (hACE2) receptor plays a central role in cell entry. We designed a series of peptides mimicking the N-terminal helix of hACE2 protein which contains most of the contacting residues at the binding site, exhibiting a high helical folding propensity in aqueous solution. Our best peptide-mimics are able to block SARS-CoV-2 human pulmonary cell infection with an inhibitory concentration (IC50) in the nanomolar range upon binding to the virus spike protein with high affinity. These first-in-class blocking peptide mimics represent powerful tools that might be used in prophylactic and therapeutic approaches to fight the coronavirus disease 2019 (COVID-19).Entities:
Year: 2021 PMID: 33580154 DOI: 10.1038/s42003-021-01736-8
Source DB: PubMed Journal: Commun Biol ISSN: 2399-3642