Autochthonous Peruvian Natural Plants as Potential SARS-CoV-2 Mpro Main Protease Inhibitors

Author:

Peralta-Moreno Maria Nuria1ORCID,Anton-Muñoz Vanessa2ORCID,Ortega-Alarcon David34ORCID,Jimenez-Alesanco Ana34,Vega Sonia3,Abian Olga3456ORCID,Velazquez-Campoy Adrian3456ORCID,Thomson Timothy M.678ORCID,Granadino-Roldán José Manuel9,Machicado Claudia38ORCID,Rubio-Martinez Jaime1ORCID

Affiliation:

1. Department of Materials Science and Physical Chemistry, University of Barcelona, and the Institut de Recerca en Quimica Teorica i Computacional (IQTCUB), 08028 Barcelona, Spain

2. Facultad de Farmacia y Bioquímica, Universidad Nacional Mayor de San Marcos, Jr. Puno 1002, Lima 15001, Peru

3. Institute of Biocomputation and Physics of Complex Systems (BIFI), Joint Unit GBsC-CSIC-BIFI, Universidad de Zaragoza, 50018 Zaragoza, Spain

4. Departamento de Bioquímica y Biología Molecular y Celular, Universidad de Zaragoza, 50009 Zaragoza, Spain

5. Instituto de Investigación Sanitaria de Aragón (IIS Aragon), 50009 Zaragoza, Spain

6. Centro de Investigación Biomédica en Red en el Área Temática de Enfermedades Hepáticas Digestivas (CIBERehd), 28029 Madrid, Spain

7. Institute of Molecular Biology of Barcelona (IBMB-CSIC), 08028 Barcelona, Spain

8. Laboratorio de Investigación Traslacional y Biología Computacional, Facultad de Ciencias y Filosofía-LID, Universidad Peruana Cayetano Heredia, Av. Honorio Delgado 430, Lima 15102, Peru

9. Departamento de Química Física y Analítica, Facultad de Ciencias Experimentales, Universidad de Jaén, Campus “Las Lagunillas” s/n, 23071 Jaén, Spain

Abstract

Over 750 million cases of COVID-19, caused by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), have been reported since the onset of the global outbreak. The need for effective treatments has spurred intensive research for therapeutic agents based on pharmaceutical repositioning or natural products. In light of prior studies asserting the bioactivity of natural compounds of the autochthonous Peruvian flora, the present study focuses on the identification SARS-CoV-2 Mpro main protease dimer inhibitors. To this end, a target-based virtual screening was performed over a representative set of Peruvian flora-derived natural compounds. The best poses obtained from the ensemble molecular docking process were selected. These structures were subjected to extensive molecular dynamics steps for the computation of binding free energies along the trajectory and evaluation of the stability of the complexes. The compounds exhibiting the best free energy behaviors were selected for in vitro testing, confirming the inhibitory activity of Hyperoside against Mpro, with a Ki value lower than 20 µM, presumably through allosteric modulation.

Funder

Agència de Gestió d’Ajuts Universitaris i de Recerca (AGAUR)-Generalitat de Catalunya

Spanish Structures and Excellence María de Maeztu program

Universitat de Barcelona PREDOCS-UB 2020

Spanish Ministry of Economy and Competitiveness

Ministry of Science and Innovation

ERDF A way of Making Europe

Fondo de Investigaciones Sanitarias from Instituto de Salud Carlos III and European Union

Diputación General de Aragón (Protein Targets and Bioactive Compounds Group

Digestive Pathology Group

Consejo Superior de Investigaciones Científicas

Plataforma Temática Interdisciplinar Salud Global

Agència de Gestió d’Ajuts Universitaris i de Recerca

Plan Nacional de I + D

Publisher

MDPI AG

Subject

Drug Discovery,Pharmaceutical Science,Molecular Medicine

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