| Literature DB >> 33564093 |
Youngchang Kim1,2, Jacek Wower3, Natalia Maltseva1,2, Changsoo Chang1,2, Robert Jedrzejczak1,2, Mateusz Wilamowski4, Soowon Kang5, Vlad Nicolaescu5, Glenn Randall5, Karolina Michalska1,2, Andrzej Joachimiak6,7,8.
Abstract
SARS-CoV-2 Nsp15 is a uridine-specific endoribonuclease with C-terminal catalytic domain belonging to the EndoU family that is highly conserved in coronaviruses. As endoribonuclease activity seems to be responsible for the interference with the innate immune response, Nsp15 emerges as an attractive target for therapeutic intervention. Here we report the first structures with bound nucleotides and show how the enzyme specifically recognizes uridine moiety. In addition to a uridine site we present evidence for a second base binding site that can accommodate any base. The structure with a transition state analog, uridine vanadate, confirms interactions key to catalytic mechanisms. In the presence of manganese ions, the enzyme cleaves unpaired RNAs. This acquired knowledge was instrumental in identifying Tipiracil, an FDA approved drug that is used in the treatment of colorectal cancer, as a potential anti-COVID-19 drug. Using crystallography, biochemical, and whole-cell assays, we demonstrate that Tipiracil inhibits SARS-CoV-2 Nsp15 by interacting with the uridine binding pocket in the enzyme's active site. Our findings provide new insights for the development of uracil scaffold-based drugs.Entities:
Year: 2021 PMID: 33564093 DOI: 10.1038/s42003-021-01735-9
Source DB: PubMed Journal: Commun Biol ISSN: 2399-3642