4.7 Article

Structural basis of SARS-CoV-2 3CL(pro) and anti-COVID-19 drug discovery from medicinal plants

Journal

JOURNAL OF PHARMACEUTICAL ANALYSIS
Volume 10, Issue 4, Pages 313-319

Publisher

ELSEVIER
DOI: 10.1016/j.jpha.2020.03.009

Keywords

Coronavirus; SARS-CoV-2; COVID-19; Natural products; Protein homology modelling; Molecular docking; Molecular dynamics simulation

Funding

  1. National Key Research and Development Program of China [2020YFC0845600]
  2. Hubei Provincial Natural Science Foundation of China [2019CFA014]
  3. Starting Research Grant for High-level Talents from Guangxi University, Nanning, China
  4. Postdoctoral Research Platform Grant of Guangxi University, Nanning, China

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The recent pandemic of coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2 has raised global health concerns. The viral 3-chymotrypsin-like cysteine protease (3CL(pro)) enzyme controls coronavirus replication and is essential for its life cycle. 3CL(pro) is a proven drug discovery target in the case of severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV). Recent studies revealed that the genome sequence of SARS-CoV-2 is very similar to that of SARS-CoV. Therefore, herein, we analysed the 3CL(pro) sequence, constructed its 3D homology model, and screened it against a medicinal plant library containing 32,297 potential anti-viral phytochemicals/traditional Chinese medicinal compounds. Our analyses revealed that the top nine hits might serve as potential anti- SARS-CoV-2 lead molecules for further optimisation and drug development process to combat COVID-19. (C) 2020 Xi'an Jiaotong University. Production and hosting by Elsevier B.V.

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