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Plant Source Derived Compound Exhibited In Silico Inhibition of Membrane Glycoprotein In SARS-CoV-2: Paving the Way to Discover a New Class of Compound For Treatment of COVID-19.
Mahanta, Saurov; Naiya, Tufan; Biswas, Kunal; Changkakoti, Liza; Mohanta, Yugal Kishore; Tanti, Bhaben; Mishra, Awdhesh Kumar; Mohanta, Tapan Kumar; Sharma, Nanaocha.
  • Mahanta S; National Institute of Electronics and Information Technology (NIELIT), Guwahati, India.
  • Naiya T; Department of Biotechnology, Maulana Abul Kalam Azad University of Technology, West Bengal, India.
  • Biswas K; Centre for Nanoscience and Nanotechnology, Sathyabama Institute of Science and Technology, Chennai, India.
  • Changkakoti L; National Institute of Electronics and Information Technology (NIELIT), Guwahati, India.
  • Mohanta YK; Department of Applied Biology, School of Biological Sciences, University of Science and Technology Meghalaya (USTM), Baridua, India.
  • Tanti B; Department of Botany, Gauhati University, Guwahati, India.
  • Mishra AK; Department of Biotechnology, Yeungnam University, Gyeongsan, South Korea.
  • Mohanta TK; Natural and Medical Sciences Research Centre, University of Nizwa, Nizwa, Oman.
  • Sharma N; Institute of Bioresources and Sustainable Development, Imphal, India.
Front Pharmacol ; 13: 805344, 2022.
Article in English | MEDLINE | ID: covidwho-1809488
ABSTRACT
SARS-CoV-2 is the virus responsible for causing COVID-19 disease in humans, creating the recent pandemic across the world, where lower production of Type I Interferon (IFN-I) is associated with the deadly form of the disease. Membrane protein or SARS-CoV-2 M proteins are known to be the major reason behind the lower production of human IFN-I by suppressing the expression of IFNß and Interferon Stimulated Genes. In this study, 7,832 compounds from 32 medicinal plants of India possessing traditional knowledge linkage with pneumonia-like disease treatment, were screened against the Homology-Modelled structure of SARS-CoV-2 M protein with the objective of identifying some active phytochemicals as inhibitors. The entire study was carried out using different modules of Schrodinger Suite 2020-3. During the docking of the phytochemicals against the SARS-CoV-2 M protein, a compound, ZIN1722 from Zingiber officinale showed the best binding affinity with the receptor with a Glide Docking Score of -5.752 and Glide gscore of -5.789. In order to study the binding stability, the complex between the SARS-CoV-2 M protein and ZIN1722 was subjected to 50 ns Molecular Dynamics simulation using Desmond module of Schrodinger suite 2020-3, during which the receptor-ligand complex showed substantial stability after 32 ns of MD Simulation. The molecule ZIN1722 also showed promising results during ADME-Tox analysis performed using Swiss ADME and pkCSM. With all the findings of this extensive computational study, the compound ZIN1722 is proposed as a potential inhibitor to the SARS-CoV-2 M protein, which may subsequently prevent the immunosuppression mechanism in the human body during the SARS-CoV-2 virus infection. Further studies based on this work would pave the way towards the identification of an effective therapeutic regime for the treatment and management of SARS-CoV-2 infection in a precise and sustainable manner.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Topics: Traditional medicine Language: English Journal: Front Pharmacol Year: 2022 Document Type: Article Affiliation country: Fphar.2022.805344

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Topics: Traditional medicine Language: English Journal: Front Pharmacol Year: 2022 Document Type: Article Affiliation country: Fphar.2022.805344