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Publication Type : Journal Article
Publisher : Saudi Journal of Biological Sciences
Source : Saudi Journal of Biological Sciences, Volume 28, Issue 1, p.1040-1051 (2021)
Url : https://pubmed.ncbi.nlm.nih.gov/33424398/
Campus : Mysuru
School : School of Arts and Sciences
Department : Sciences
Year : 2021
Abstract : The novel coronavirus pandemic has spread over in 213 countries as of July 2020. Approximately 12 million people have been infected so far according to the reports from World Health Organization (WHO). Preventive measures are being taken globally to avoid the rapid spread of virus. In the current study, an approach is carried out as a means of inhibiting the spike protein of the novel coronavirus by flavonoids from natural sources that possess both antiviral and anti-inflammatory properties. The methodology is focused on molecular docking of 10 flavonoid compounds that are docked with the spike protein of SARS-CoV-2, to determine the highest binding affinity at the binding site. Molecular dynamics simulation was carried out with the flavonoid-protein complex showing the highest binding affinity and highest interactions. The flavonoid naringin showed the least binding energy of -9.8 Kcal/mol with the spike protein which was compared with the standard drug, dexamethasone which is being repurposed to treat critically ill patients. MD simulation was carried out on naringin-spike protein complex for their conformational stability in the active site of the novel coronavirus spike protein. The RMSD of the complex appeared to be more stable when compared to that of the protein from 0.2 nm to 0.4 nm. With the aid of this approach further studies can be carried out on these flavonoids against the novel coronavirus as a means of viral protein inhibitors.
Cite this Research Publication : A. S. Jain, Sushma, P., Dharmashekar, C., Beelagi, M. S., Prasad, S. K., Shivamallu, C., Prasad, A., Syed, A., Marraiki, N., and Shiva Prasad Kollur, “In silico evaluation of flavonoids as effective antiviral agents on the spike glycoprotein of SARS-CoV-2”, Saudi Journal of Biological Sciences, vol. 28, no. 1, pp. 1040-1051, 2021.