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Identifying SARS-CoV-2 antiviral compounds by screening for small molecule inhibitors of nsp13 helicase.

Authors :
Jingkun Zeng
Weissmann, Florian
Bertolin, Agustina P.
Posse, Viktor
Canal, Berta
Ulferts, Rachel
Wu, Mary
Harvey, Ruth
Hussain, Saira
Milligan, Jennifer C.
Roustan, Chloe
Borg, Annabel
McCoy, Laura
Drury, Lucy S.
Kjaer, Svend
McCauley, John
Howell, Michael
Beale, Rupert
Diffley, John F. X.
Source :
Biochemical Journal. Jul2021, Vol. 478 Issue 13, p2405-2423. 19p.
Publication Year :
2021

Abstract

The coronavirus disease 2019 (COVID-19) pandemic, which is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is a global public health challenge. While the efficacy of vaccines against emerging and future virus variants remains unclear, there is a need for therapeutics. Repurposing existing drugs represents a promising and potentially rapid opportunity to find novel antivirals against SARS-CoV-2. The virus encodes at least nine enzymatic activities that are potential drug targets. Here, we have expressed, purified and developed enzymatic assays for SARS-CoV-2 nsp13 helicase, a viral replication protein that is essential for the coronavirus life cycle. We screened a custom chemical library of over 5000 previously characterized pharmaceuticals for nsp13 inhibitors using a fluorescence resonance energy transfer-based high-throughput screening approach. From this, we have identified FPA-124 and several suramin-related compounds as novel inhibitors of nsp13 helicase activity in vitro. We describe the efficacy of these drugs using assays we developed to monitor SARS-CoV-2 growth in Vero E6 cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02646021
Volume :
478
Issue :
13
Database :
Academic Search Index
Journal :
Biochemical Journal
Publication Type :
Academic Journal
Accession number :
151692022
Full Text :
https://doi.org/10.1042/BCJ20210201