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In Silico Analysis of Honeybee Venom Protein Interaction with Wild Type and Mutant (A82V + P375S) <em>Ebola</em> Virus Spike Protein
oleh: Muhammad Muzammal, Muzammil Ahmad Khan, Mohammed Al Mohaini, Abdulkhaliq J. Alsalman, Maitham A. Al Hawaj, Arshad Farid
Format: | Article |
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Diterbitkan: | MDPI AG 2022-01-01 |
Deskripsi
Venom from different organisms was used in ancient times to treat a wide range of diseases, and to combat a variety of enveloped and non-enveloped viruses. The aim of this in silico research was to investigate the impact of honeybee venom proteins and peptides against <i>Ebola</i> virus. In the current in silico study, different online and offline tools were used. RaptorX (protein 3D modeling) and PatchDock (protein–protein docking) were used as online tools, while Chimera and LigPlot + v2.1 were used for visualizing protein–protein interactions. We screened nine venom proteins and peptides against the normal <i>Ebola</i> virus spike protein and found that melittin, MCD and phospholipase A2 showed a strong interaction. We then screened these peptides and proteins against mutated strains of Ebola virus and found that the enzyme phospholipase A2 showed a strong interaction. According to the findings, phospholipase A2 found in honeybee venom may be an effective source of antiviral therapy against the deadly <i>Ebola</i> virus. Although the antiviral potency of phospholipase A2 has been recorded previously, this is the first in silico analysis of honeybee phospholipase A2 against the <i>Ebola</i> viral spike protein and its more lethal mutant strain.