tetano
Editor, Senior Moderator
ACS Catal. 2020;10:5871-5890. doi: 10.1021/acscatal.0c00110. Epub 2020 Apr 28.
Comprehensive Insights into the Catalytic Mechanism of Middle East Respiratory Syndrome 3C-Like Protease and Severe Acute Respiratory Syndrome 3C-Like Protease.
Wang H[SUP]1,[/SUP][SUP]2[/SUP], He S[SUP]1,[/SUP][SUP]2[/SUP], Deng W[SUP]1,[/SUP][SUP]2[/SUP], Zhang Y[SUP]3[/SUP], Li G[SUP]1,[/SUP][SUP]2[/SUP], Sun J[SUP]1[/SUP], Zhao W[SUP]1,[/SUP][SUP]2[/SUP], Guo Y[SUP]1,[/SUP][SUP]2[/SUP], Yin Z[SUP]1,[/SUP][SUP]2,[/SUP][SUP]4[/SUP], Li D[SUP]1[/SUP], Shang L[SUP]1,[/SUP][SUP]2[/SUP].
Author information
Abstract
Coronavirus 3C-like protease (3CL[SUP]Pro[/SUP]) is a highly conserved cysteine protease employing a catalytic dyad for its functions. 3CL[SUP]Pro[/SUP] is essential to the viral life cycle and, therefore, is an attractive target for developing antiviral agents. However, the detailed catalytic mechanism of coronavirus 3CL[SUP]Pro[/SUP] remains largely unknown. We took an integrated approach of employing X-ray crystallography, mutational studies, enzyme kinetics study, and inhibitors to gain insights into the mechanism. Such experimental work is supplemented by computational studies, including the prereaction state analysis, the ab initio calculation of the critical catalytic step, and the molecular dynamic simulation of the wild-type and mutant enzymes. Taken together, such studies allowed us to identify a residue pair (Glu-His) and a conserved His as critical for binding; a conserved GSCGS motif as important for the start of catalysis, a partial negative charge cluster (PNCC) formed by Arg-Tyr-Asp as essential for catalysis, and a conserved water molecule mediating the remote interaction between PNCC and catalytic dyad. The data collected and our insights into the detailed mechanism have allowed us to achieve a good understanding of the difference in catalytic efficiency between 3CL[SUP]Pro[/SUP] from SARS and MERS, conduct mutational studies to improve the catalytic activity by 8-fold, optimize existing inhibitors to improve the potency by 4-fold, and identify a potential allosteric site for inhibitor design. All such results reinforce each other to support the overall catalytic mechanism proposed herein.
Copyright ? 2020 American Chemical Society.
PMID:32391184PMCID:PMC7202269DOI:10.1021/acscatal.0c00110
Comprehensive Insights into the Catalytic Mechanism of Middle East Respiratory Syndrome 3C-Like Protease and Severe Acute Respiratory Syndrome 3C-Like Protease.
Wang H[SUP]1,[/SUP][SUP]2[/SUP], He S[SUP]1,[/SUP][SUP]2[/SUP], Deng W[SUP]1,[/SUP][SUP]2[/SUP], Zhang Y[SUP]3[/SUP], Li G[SUP]1,[/SUP][SUP]2[/SUP], Sun J[SUP]1[/SUP], Zhao W[SUP]1,[/SUP][SUP]2[/SUP], Guo Y[SUP]1,[/SUP][SUP]2[/SUP], Yin Z[SUP]1,[/SUP][SUP]2,[/SUP][SUP]4[/SUP], Li D[SUP]1[/SUP], Shang L[SUP]1,[/SUP][SUP]2[/SUP].
Author information
Abstract
Coronavirus 3C-like protease (3CL[SUP]Pro[/SUP]) is a highly conserved cysteine protease employing a catalytic dyad for its functions. 3CL[SUP]Pro[/SUP] is essential to the viral life cycle and, therefore, is an attractive target for developing antiviral agents. However, the detailed catalytic mechanism of coronavirus 3CL[SUP]Pro[/SUP] remains largely unknown. We took an integrated approach of employing X-ray crystallography, mutational studies, enzyme kinetics study, and inhibitors to gain insights into the mechanism. Such experimental work is supplemented by computational studies, including the prereaction state analysis, the ab initio calculation of the critical catalytic step, and the molecular dynamic simulation of the wild-type and mutant enzymes. Taken together, such studies allowed us to identify a residue pair (Glu-His) and a conserved His as critical for binding; a conserved GSCGS motif as important for the start of catalysis, a partial negative charge cluster (PNCC) formed by Arg-Tyr-Asp as essential for catalysis, and a conserved water molecule mediating the remote interaction between PNCC and catalytic dyad. The data collected and our insights into the detailed mechanism have allowed us to achieve a good understanding of the difference in catalytic efficiency between 3CL[SUP]Pro[/SUP] from SARS and MERS, conduct mutational studies to improve the catalytic activity by 8-fold, optimize existing inhibitors to improve the potency by 4-fold, and identify a potential allosteric site for inhibitor design. All such results reinforce each other to support the overall catalytic mechanism proposed herein.
Copyright ? 2020 American Chemical Society.
PMID:32391184PMCID:PMC7202269DOI:10.1021/acscatal.0c00110