Related Experiment Video
Updated: May 10, 2025

Analysis of Group IV Viral SSHHPS Using In Vitro and In Silico Methods
Published on: December 21, 2019
Elucidating the structural dynamics induced by active site mutations in 3C protease of foot-and-mouth disease virus
Sthitaprajna Sahoo1, Hak-Kyo Lee1,2, Donghyun Shin1
1Department of Agricultural Convergence Technology, Jeonbuk National University, Jeonju, Republic of Korea.
Abstract:
The viral replication of foot-and-mouth disease virus (FMDV) and other picornaviruses primarily depends on the successful processing of a polyprotein precursor by the enzyme 3C protease (3Cpro) at specific sites. The crucial role of 3Cpro in viral replication and pathogenesis makes it a potential target for developing novel therapeutics against foot-and-mouth disease. The β-ribbon region (residues 138-150) containing the active site residues (C142) in 3Cpro is found to be conserved and contributes significantly to substrate specificity. Moreover, experimental reports suggest that mutations at position 142, particularly C142S and C142L, exhibit different functional activities. However, the intrinsic dynamics and conformational changes induced by active-site mutations of 3Cpro remain unclear, limiting the development of novel inhibitors of 3C protease. Accordingly, we carried out molecular dynamics (MD) simulations with multiple replicates for both the WT and mutants of 3Cpro. The observed results suggest that the C142S mutant induces substantial structural transitions compared to the WT and C142L. In contrast, the essential dynamics of the mutants significantly varied from those of the WT 3Cpro. Moreover, cross-correlation analysis revealed a similar pattern of anti-correlation between the amino acid residues of the WT and C142L mutant complexes. Analysis of the betweenness centrality of the WT and the mutants from the residue interaction networks revealed common residues for intra-residual signal propagation. The results from our study suggest that the active site mutant C142S may induce conformational changes, which can cause the β-ribbon region to bend towards the catalytic pocket and inhibit the enzymatic activity. C142L substitution may also alter the β-ribbon region conformation, which may impact the substrate binding process during proteolysis, as reported in previous studies. These results can provide a better understanding of the conformational dynamic behavior of 3Cpro active-site mutants and may assist in developing potential inhibitors against foot-and-mouth disease.
Insights
Foot-and-mouth disease virus 3C protease (3Cpro) mutations C142S and C142L were studied using molecular dynamics. The C142S mutant showed significant structural changes, impacting enzyme activity and offering insights for novel antiviral therapies.
Area of Science:
- Biochemistry
- Structural Biology
- Virology
Background:
- Foot-and-mouth disease virus (FMDV) replication relies on 3C protease (3Cpro) for polyprotein processing.
- 3Cpro is a key target for developing FMDV therapeutics.
- The conserved β-ribbon region and active site residue C142 are critical for 3Cpro function.
Purpose of the Study:
- To investigate the intrinsic dynamics and conformational changes of FMDV 3Cpro active-site mutants (C142S and C142L).
- To elucidate how these mutations affect 3Cpro structure and function, aiding in the design of new inhibitors.
Main Methods:
- Molecular dynamics (MD) simulations with multiple replicates were performed on wild-type (WT) 3Cpro and its C142S and C142L mutants.
- Analysis included essential dynamics, cross-correlation, and residue interaction networks (betweenness centrality).
Main Results:
- The C142S mutant exhibited substantial structural transitions and altered essential dynamics compared to WT and C142L.
- C142L showed similar residue anti-correlation patterns to WT, suggesting distinct functional impacts.
- Signal propagation pathways were identified in WT and mutant 3Cpro.
Conclusions:
- The C142S mutation may inhibit 3Cpro activity by inducing conformational changes that bend the β-ribbon region towards the catalytic pocket.
- The C142L substitution might affect substrate binding by altering β-ribbon conformation.
- Understanding these dynamic behaviors aids in developing effective foot-and-mouth disease inhibitors.
More Related Videos
07:53A Fluorogenic Peptide Cleavage Assay to Screen for Proteolytic Activity: Applications for coronavirus spike protein activation
Published on: January 9, 2019
08:40Production of Pseudotyped Particles to Study Highly Pathogenic Coronaviruses in a Biosafety Level 2 Setting
Published on: March 1, 2019
Related Concept Videos
Induced-fit Model
Enzymes exhibit substrate specificity, meaning that they can only bind to certain substrates. This is mainly determined by the shape and chemical...
Introduction to Mechanisms of Enzyme Catalysis
Enzymes
Enzyme deficiencies can often translate into life-threatening diseases. For example, a genetic abnormality resulting in the deficiency of the enzyme G6PD...
Viral Mutations
Viral Structure
Mechanical Protein Function