Computational Drug Design against Ebola Virus Targeting Viral Matrix Protein VP30
DOI:
https://doi.org/10.33084/bjop.v2i2.836Keywords:
Ebola Virus, VP30, Molecular Docking, Molecular Dynamics Simulation, Drug DesignAbstract
Ebola viral disease (EVD) is a deadly infectious hemorrhagic viral fever caused by the Ebola virus with a high mortality rate. Until date, there is no effective drug or vaccination available to combat this condition. This study focuses on designing an effective antiviral drug for Ebola viral disease targeting viral protein 30 (VP30) of Ebola virus, highly required for transcription initiation. The lead molecules were screened for Lipinski rule of five, ADMET study following which molecular docking and bioactivity prediction was carried out. The compounds with the least binding energy were analyzed using interaction software. The results revealed that 6-Hydroxyluteolin and (-)-Arctigenin represent active lead compounds that inhibit the activity of VP30 protein and exhibits efficient pharmacokinetics. Both these compounds are plant-derived flavonoids and possess no known adverse effects on human health. In addition, they bind strongly to the predicted binding site centered on Lys180, suggesting that these two lead molecules can be imperative in designing a potential drug for EVD.
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Copyright (c) 2019 Arthi Venkatesan, Lavanya Ravichandran, J Febin Prabhu Dass
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