Crystal structures of main protease ($ M^{pro} $) mutants of SARS-CoV-2 variants bound to PF-07304814

Abstract There is an urgent need to develop effective antiviral drugs to prevent the viral infection caused by constantly circulating SARS-CoV-2 as well as its variants. The main protease ($ M^{pro} $) of SARS-CoV-2 is a salient enzyme that plays a vital role in viral replication and serves as a fas...
Ausführliche Beschreibung

Abstract There is an urgent need to develop effective antiviral drugs to prevent the viral infection caused by constantly circulating SARS-CoV-2 as well as its variants. The main protease ($ M^{pro} $) of SARS-CoV-2 is a salient enzyme that plays a vital role in viral replication and serves as a fascinating therapeutic target. PF-07304814 is a covalent inhibitor targeting SARS-CoV-2 $ M^{pro} $ with favorable inhibition potency and drug-like properties, thus making it a promising drug candidate for the treatment of COVID-19. We previously solved the structure of PF-07304814 in complex with SARS-CoV-2 $ M^{pro} $. However, the binding modes of PF-07304814 with $ M^{pro} $s from evolving SARS-CoV-2 variants is under-determined. In the current study, we expressed six $ M^{pro} $ mutants (G15S, K90R, M49I, S46F, V186F, and Y54C) that have been identified in Omicron variants including the recently emerged XBB.1.16 subvariant and solved the crystal structures of PF-07304814 bound to $ M^{pro} $ mutants. Structural analysis provided insight into the key molecular determinants responsible for the interaction between PF-07304814 and these mutant $ M^{pro} $s. Patterns for PF-07304814 to bind with these investigated $ M^{pro} $ mutants and the wild-type $ M^{pro} $ are generally similar but with some differences as revealed by detailed structural comparison. Structural insights presented in this study will inform the development of novel drugs against SARS-CoV-2 and the possible conformation changes of $ M^{pro} $ mutants when bound to an inhibitor. Ausführliche Beschreibung