J Biomol Struct Dyn. Using Integrated Computational Approaches to Identify Safe and Rapid Treatment for SARS -CoV- 2

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J Biomol Struct Dyn. 2020 May 4:1-11. doi: 10.1080/07391102.2020.1764392. [Epub ahead of print]
Using Integrated Computational Approaches to Identify Safe and Rapid Treatment for SARS -CoV- 2.


Al-Khafaji K¹, Al-DuhaidahawiL D², Taskin Tok T^1,3.

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Abstract

SARS-CoV-2 is a new generation of coronavirus, which was firstly determined in Wuhan, China, in December 2019. So far, however, there no effective treatment has been found to stop this new generation of coronavirus but discovering of the crystal structure of SARS-CoV-2 main protease (SARS-CoV-2 M pro) may facilitate searching for new therapies for SARS-COV-2 . The aim was to assess the effectiveness of available FDA approved drugs which can construct a covalent bond with Cys145 inside binding site SARS-CoV-2 main protease by using covalent docking screening.
METHOD:

We conducted the covdock module MMGBSA module in the Schrodinger suite 2020-1, to examine the covalent bonding utilizing. Besides, we submitted the top three drugs to molecular dynamics simulations via Gromacs 2018.1.
RESULTS:

The covalent docking showed that saquinavir, ritonavir, remdesivir, delavirdine, cefuroxime axetil, oseltamivir and prevacid have the highest binding energies MMGBSA of -72.17, -72.02, -65.19, -57.65, -54.25, -51.8, -51.14 kCal/mol, respectively. 50 ns molecular dynamics simulation was conducted for saquinavir, ritonavir and remdesivir to evaluate the stability of these drugs inside the binding pocket of SARS-CoV-2 main protease.
CONCLUSION:

The current study provides a powerful in silico results, means for rapid screening of drugs as anti-protease medications and recommend that the above-mentioned drugs can be used in the treatment of SARS-CoV-2 in combined or sole therapy.



KEYWORDS:

Covalent Docking; Drug repurposing; M pro; MD simulation; PCA; SARS-CoV-2


PMID:32364041DOI:10.1080/07391102.2020.1764392