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Unveiling mutation effects on the structural dynamics of the main protease from SARS-CoV-2 with hybrid simulation methods.

Authors :
Gasparini P
Philot EA
Pantaleão SQ
Torres-Bonfim NESM
Kliousoff A
Quiroz RCN
Perahia D
Simões RP
Magro AJ
Scott AL
Source :
Journal of molecular graphics & modelling [J Mol Graph Model] 2023 Jun; Vol. 121, pp. 108443. Date of Electronic Publication: 2023 Feb 22.
Publication Year :
2023

Abstract

The main protease of SARS-CoV-2 (called M <superscript>pro</superscript> or 3CL <superscript>pro</superscript> ) is essential for processing polyproteins encoded by viral RNA. Several M <superscript>pro</superscript> mutations were found in SARS-CoV-2 variants, which are related to higher transmissibility, pathogenicity, and resistance to neutralization antibodies. Macromolecules adopt several favored conformations in solution depending on their structure and shape, determining their dynamics and function. In this study, we used a hybrid simulation method to generate intermediate structures along the six lowest frequency normal modes and sample the conformational space and characterize the structural dynamics and global motions of WT SARS-CoV-2 M <superscript>pro</superscript> and 48 mutations, including mutations found in P.1, B.1.1.7, B.1.351, B.1.525 and B.1.429+B.1.427 variants. We tried to contribute to the elucidation of the effects of mutation in the structural dynamics of SARS-CoV-2 M <superscript>pro</superscript> . A machine learning analysis was performed following the investigation regarding the influence of the K90R, P99L, P108S, and N151D mutations on the dimeric interface assembling of the SARS-CoV-2 M <superscript>pro</superscript> . The parameters allowed the selection of potential structurally stable dimers, which demonstrated that some single surface aa substitutions not located at the dimeric interface (K90R, P99L, P108S, and N151D) are able to induce significant quaternary changes. Furthermore, our results demonstrated, by a Quantum Mechanics method, the influence of SARS-CoV-2 M <superscript>pro</superscript> mutations on the catalytic mechanism, confirming that only one of the chains of the WT and mutant SARS-CoV-2 M <superscript>pro</superscript> s are prone to cleave substrates. Finally, it was also possible to identify the aa residue F140 as an important factor related to the increasing enzymatic reactivity of a significant number of SARS-CoV-2 M <superscript>pro</superscript> conformations generated by the normal modes-based simulations.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Ana ligia Scott reports financial support was provided by National Council for Scientific and Technological Development.<br /> (Copyright © 2023 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-4243
Volume :
121
Database :
MEDLINE
Journal :
Journal of molecular graphics & modelling
Publication Type :
Academic Journal
Accession number :
36870228
Full Text :
https://doi.org/10.1016/j.jmgm.2023.108443