期刊
BIOCHEMICAL JOURNAL
卷 478, 期 1, 页码 2499-2515出版社
PORTLAND PRESS LTD
DOI: 10.1042/BCJ20210197
关键词
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资金
- Francis Crick Institute from Cancer Research U.K. [FC001066]
- U.K. Medical Research Council [FC001066]
- Wellcome Trust [FC001066]
Research has been conducted on the main viral protease of SARS-CoV-2, leading to the identification of several inhibitors that show strong inhibitory effects on the virus activity in vitro. These inhibitors have the potential to become promising antiviral drugs.
The coronavirus 2019 (COVID-19) pandemic, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), spread around the world with unprecedented health and socio-economic effects for the global population. While different vaccines are now being made available, very few antiviral drugs have been approved. The main viral protease (nsp5) of SARS-CoV-2 provides an excellent target for antivirals, due to its essential and conserved function in the viral replication cycle. We have expressed, purified and developed assays for nsp5 protease activity. We screened the nsp5 protease against a custom chemical library of over 5000 characterised pharmaceuticals. We identified calpain inhibitor I and three different peptidyl fluoromethylketones (FMK) as inhibitors of nsp5 activity in vitro, with IC50 values in the low micromolar range. By altering the sequence of our peptidomimetic FMK inhibitors to better mimic the substrate sequence of nsp5, we generated an inhibitor with a subnanomolar IC50. Calpain inhibitor I inhibited viral infection in monkey-derived Vero E6 cells, with an EC50 in the low micromolar range. The most potent and commercially available peptidyl-FMK compound inhibited viral growth in Vero E6 cells to some extent, while our custom peptidyl FMK inhibitor offered a marked antiviral improvement.
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