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Identifying SARS-CoV-2 Antiviral Compounds by Screening for Small Molecule Inhibitors of Nsp13 Helicase
Rupert Beale; Agustina P Bertolin; Annabel Borg; Berta Canal; John FX Diffley; Lucy S Drury; Ruth Harvey; Michael Howell; Saira Hussain; Svend Kjaer; John McCauley; Laura McCoy; Jennifer Milligan; Viktor Posse; Rachel Ulferts; Florian Weissmann; Mary Wu; Jingkun Zeng.
Affiliation
  • Rupert Beale; The Francis Crick Institute
  • Agustina P Bertolin; The Francis Crick Institute
  • Annabel Borg; The Francis Crick Institute
  • Berta Canal; The Francis Crick Institute
  • John FX Diffley; The Francis Crick Institute
  • Lucy S Drury; The Francis Crick Institute
  • Ruth Harvey; The Francis Crick Institute
  • Michael Howell; The Francis Crick Institute
  • Saira Hussain; The Francis Crick Institute
  • Svend Kjaer; The Francis Crick Institute
  • John McCauley; The Francis Crick Institute
  • Laura McCoy; University College London
  • Jennifer Milligan; The Francis Crick Institute
  • Viktor Posse; The Francis Crick Institute
  • Rachel Ulferts; The Francis Crick Institute
  • Florian Weissmann; The Francis Crick Institute
  • Mary Wu; The Francis Crick Institute
  • Jingkun Zeng; The Francis Crick Institute
Preprint in En | PREPRINT-BIORXIV | ID: ppbiorxiv-438808
Journal article
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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 characterised pharmaceuticals for nsp13 inhibitors using a FRET-based high-throughput screening (HTS) 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.
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Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2021 Document type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2021 Document type: Preprint