| Literature DB >> 33574416 |
Ewelina Weglarz-Tomczak1, Jakub M Tomczak2, Michał Talma3, Małgorzata Burda-Grabowska3,4, Mirosław Giurg4, Stanley Brul5.
Abstract
An efficient treatment against a COVID-19 disease, caused by the novel coronavirus SARS-CoV-2 (CoV2), remains a challenge. The papain-like protease (PLpro) from the human coronavirus is a protease that plays a critical role in virus replication. Moreover, CoV2 uses this enzyme to modulate the host's immune system to its own benefit. Therefore, it represents a highly promising target for the development of antiviral drugs. We used Approximate Bayesian Computation tools, molecular modelling and enzyme activity studies to identify highly active inhibitors of the PLpro. We discovered organoselenium compounds, ebselen and its structural analogues, as a novel approach for inhibiting the activity of PLproCoV2. Furthermore, we identified, for the first time, inhibitors of PLproCoV2 showing potency in the nanomolar range. Moreover, we found a difference between PLpro from SARS and CoV2 that can be correlated with the diverse dynamics of their replication, and, putatively to disease progression.Entities:
Year: 2021 PMID: 33574416 PMCID: PMC7878891 DOI: 10.1038/s41598-021-83229-6
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379