期刊
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS
卷 40, 期 22, 页码 12347-12357出版社
TAYLOR & FRANCIS INC
DOI: 10.1080/07391102.2021.1970626
关键词
COVID-19; main protease; M-pro; Molecular dynamics simulation
资金
- CNPq [447120/2014-0]
- FAPESP [2016/12899-6, 2019/24112-9]
- CNPq, Brazil
- FAPESP, Brazil
This study explored the interaction and conformational changes of SARS-CoV-2 main protease (M-pro) with ligands through molecular dynamics simulations. The results showed that the dimeric form of Mpro had stable interactions with ligands, while the monomeric form exhibited unrealistic flexibility. Additionally, the interactions with residues His41, Gly143, His163, Glu166, and Gln189 were postulated to significantly affect the inhibitory activity of the ligands.
SARS-CoV-2's main protease (M-pro) interaction with ligands has been explored with a myriad of crystal structures, most of the monomers. Nonetheless, Mpro is known to be active as a dimer but the relevance of the dimerization in the ligand-induced conformational changes has not been fully elucidated. We systematically simulated different Mpro-ligand complexes aiming to study their conformational changes and interactions, through molecular dynamics (MD). We focused on covalently bound ligands (N1 and N3, similar to 9 ls per system both monomers and dimers) and compared these trajectories against the apostructure. Our results suggest that the monomeric simulations led to an unrealistically flexible active site. In contrast, the Mpro dimer displayed a stable oxyanion-loop conformation along the trajectory. Also, ligand interactions with residues His41, Gly143, His163, Glu166 and Gln189 are postulated to impact the ligands' inhibitory activity significantly. In dimeric simulations, especially Gly143 and His163 have increased interaction frequencies. In conclusion, long-timescale MD is a more suitable tool for exploring in silico the activity of bioactive compounds that potentially inhibit the dimeric form of SARS-CoV-2 Mpro.
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