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Binding of inhibitors to the monomeric and dimeric SARS-CoV-2 Mpro.

ABSTRACT: SARS-CoV-2 rapidly infects millions of people worldwide since December 2019. There is still no effective treatment for the virus, resulting in the death of more than one million patients. Inhibiting the activity of SARS-CoV-2 main protease (Mpro), 3C-like protease (3CLP), is able to block the viral replication and proliferation. In this context, our study has revealed that in silico screening for inhibitors of SARS-CoV-2 Mpro can be reliably done using the monomeric structure of the Mpro instead of the dimeric one. Docking and fast pulling of ligand (FPL) simulations for both monomeric and dimeric forms correlate well with the corresponding experimental binding affinity data of 24 compounds. The obtained results were also confirmed via binding pose and noncovalent contact analyses. Our study results show that it is possible to speed up computer-aided drug design for SARS-CoV-2 Mpro by focusing on the monomeric form instead of the larger dimeric one.

SUBMITTER: Tam NM

PROVIDER: S-EPMC8694027 | biostudies-literature | 2021 Jan

REPOSITORIES: biostudies-literature

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Binding of inhibitors to the monomeric and dimeric SARS-CoV-2 Mpro.

Tam Nguyen Minh NM Nam Pham Cam PC Quang Duong Tuan DT Tung Nguyen Thanh NT Vu Van V VV Ngo Son Tung ST

RSC advances 20210113 5

SARS-CoV-2 rapidly infects millions of people worldwide since December 2019. There is still no effective treatment for the virus, resulting in the death of more than one million patients. Inhibiting the activity of SARS-CoV-2 main protease (Mpro), 3C-like protease (3CLP), is able to block the viral replication and proliferation. In this context, our study has revealed that <i>in silico</i> screening for inhibitors of SARS-CoV-2 Mpro can be reliably done using the monomeric structure of the Mpro ...[more]

PMID: 35424256

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