Journal Article

Exploration of Microbially Derived Natural Compounds against Monkeypox Virus as Viral Core Cysteine Proteinase Inhibitors

Alawi, Maha M., Altwaim, Sarah A., Dubey, Amit, Alandijany, Thamir A., Sahoo, Amaresh Kumar, Dwivedi, Vivek Dhar, Alsaady, Isra M., Azhar, Esam Ibraheem

2023

Overview

Monkeypox virus (MPXV) is a member of the Orthopoxvirus genus and the Poxviridae family, which instigated a rising epidemic called monkeypox disease. Proteinases are majorly engaged in viral propagation by catalyzing the cleavage of precursor polyproteins. Therefore, proteinase is essential for monkeypox and a critical drug target. In this study, high-throughput virtual screening (HTVS) and molecular dynamics simulation were applied to detect the potential natural compounds against the proteinase of the monkeypox virus. Here, 32,552 natural products were screened, and the top five compounds were selected after implementing the HTVS and molecular docking protocols in series. Gallicynoic Acid F showed the minimum binding score of −10.56 kcal/mole in the extra precision scoring method, which reflected the highest binding with the protein. The top five compounds showed binding scores ≤−8.98 kcal/mole. These compound complexes were tested under 100 ns molecular dynamics simulation, and Vaccinol M showed the most stable and consistent RMSD trend in the range of 2 Å to 3 Å. Later, MM/GBSA binding free energy and principal component analysis were performed on the top five compounds to validate the stability of selected compound complexes. Moreover, the ligands Gallicynoic Acid F and H2-Erythro-Neopterin showed the lowest binding free energies of −61.42 kcal/mol and −61.09 kcal/mol, respectively. Compared to the native ligand TTP-6171 (ΔGBind = −53.86 kcal/mol), these two compounds showed preferable binding free energy, suggesting inhibitory application against MPXV proteinase. This study proposed natural molecules as a therapeutic solution to control monkeypox disease.

• Publisher: MDPI AG,MDPI
• Subject: Antiviral Agents - pharmacology / antivirals / Binding sites / Biological Products - pharmacology / Cysteine proteinase / Cysteine Proteinase Inhibitors / cysteine proteinases / Drug resistance / drugs / Epidemics / FDA approval / Free energy / Gibbs free energy / Humans / Ligands / Molecular Docking Simulation / Molecular dynamics / Molecular Dynamics Simulation / Monkeypox virus / Monkeypox virus - drug effects / Mpox / Mpox (monkeypox) / Natural products / Neopterin / Peptide Hydrolases / Polyproteins / principal component analysis / Principal components analysis / Proteinase inhibitors / Proteins / Simulation / Smallpox / Therapeutic targets / therapeutics / virtual screening / Viruses