Abstract
The human-to-human transmitted respiratory illness in COVID-19 affected by the pathogenic Severe Acute Respiratory Syndrome Corona Virus 2 (SARS-CoV-2), which appeared in the last of December 2019 in Wuhan, China, and rapidly spread in many countries. Thereon, based on the urgent need for therapeutic molecules, we conducted in silico based docking and simulation molecular interaction studies on repurposing drugs, targeting SARS-CoV-2 spike protein. Further, the best binding energy of doxorubicin interacting with virus spike protein (PDB: 6VYB) was observed to be −6.38 kcal/mol and it was followed by exemestane and gatifloxacin. The molecular simulation dynamics analysis of doxorubicin, Reference Mean Square Deviation (RMSD), Root Mean Square fluctuation (RMSF), Radius of Gyration (Rg), and formation of hydrogen bonds plot interpretation suggested, a significant deviation and fluctuation of Doxorubicin-Spike RBD complex during the whole simulation period. The Rg analysis has stated that the Doxorubicin-Spike RBD complex was stable during 15,000–35,000 ps MDS. The results have suggested that doxorubicin could inhibit the virus spike protein and prevent the access of the SARS-CoV-2 to the host cell. Thus, in-vitro/in-vivo research on these drugs could be advantageous to evaluate significant molecules that control the COVID-19 disease.
【저자키워드】 SARS-CoV-2, pandemic, antiviral drugs, Spike protein, Exemestane, Doxorubicin, Gatifloxacin, 【초록키워드】 COVID-19, drugs, Respiratory illness, drug, docking, in silico, binding energy, COVID-19 disease, Spread, Corona, SARS-CoV-2 spike protein, Research, Interpretation, respiratory, Molecular simulation, Hydrogen bond, RMSD, RMSF, Analysis, host cell, root, pathogenic, molecular interaction, gyration, radius, deviation, virus spike protein, therapeutic molecules, RBD complex, MDs, Prevent, reference, fluctuation, Wuhan, China, square, affected, evaluate, transmitted, inhibit, conducted, suggested, the SARS-CoV-2, 【제목키워드】 SARS-CoV-2 spike protein, Interaction, Simulation study, drugs targeting,