| Literature DB >> 33381049 |
Charlie Nichols1,2, Joseph Ng1, Annika Keshu1, Franca Fraternali1, Gian F De Nicola1,2.
Abstract
In-crystal fragment screening is a powerful tool to chemically probe the surfaces used by proteins to interact, and identify the chemical space worth exploring to design protein-protein inhibitors. A crucial prerequisite is the identification of a crystal form where the target area is exposed and accessible to be probed by fragments. Here we report a crystal form of the SARS-CoV-2 Receptor Binding Domain in complex with the CR3022 antibody where the ACE2 binding site on the Receptor Binding Domain is exposed and accessible. This crystal form of the complex is a valuable tool to develop antiviral molecules that could act by blocking the virus entry in cells.Entities:
Keywords: CR3022; PPI inhibitors; SARC-CoV-2-RBD; drug discovery; in-crystal fragment screening
Year: 2020 PMID: 33381049 PMCID: PMC7768231 DOI: 10.3389/fphar.2020.615211
Source DB: PubMed Journal: Front Pharmacol ISSN: 1663-9812 Impact factor: 5.810