TY - JOUR
T1 - AI-driven drug repurposing and binding pose meta dynamics identifies novel targets for monkeypox virus
AU - Patel, Chirag N.
AU - Mall, Raghvendra
AU - Bensmail, Halima
N1 - Publisher Copyright:
© 2023 The Authors
PY - 2023/5
Y1 - 2023/5
N2 - Monkeypox virus (MPXV) was confirmed in May 2022 and designated a global health emergency by WHO in July 2022. MPX virions are big, enclosed, brick-shaped, and contain a linear, double-stranded DNA genome as well as enzymes. MPXV particles bind to the host cell membrane via a variety of viral-host protein interactions. As a result, the wrapped structure is a potential therapeutic target. DeepRepurpose, an artificial intelligence-based compound-viral proteins interaction framework, was used via a transfer learning setting to prioritize a set of FDA approved and investigational drugs which can potentially inhibit MPXV viral proteins. To filter and narrow down the lead compounds from curated collections of pharmaceutical compounds, we used a rigorous computational framework that included homology modeling, molecular docking, dynamic simulations, binding free energy calculations, and binding pose metadynamics. We identified Elvitegravir as a potential inhibitor of MPXV virus using our comprehensive pipeline.
AB - Monkeypox virus (MPXV) was confirmed in May 2022 and designated a global health emergency by WHO in July 2022. MPX virions are big, enclosed, brick-shaped, and contain a linear, double-stranded DNA genome as well as enzymes. MPXV particles bind to the host cell membrane via a variety of viral-host protein interactions. As a result, the wrapped structure is a potential therapeutic target. DeepRepurpose, an artificial intelligence-based compound-viral proteins interaction framework, was used via a transfer learning setting to prioritize a set of FDA approved and investigational drugs which can potentially inhibit MPXV viral proteins. To filter and narrow down the lead compounds from curated collections of pharmaceutical compounds, we used a rigorous computational framework that included homology modeling, molecular docking, dynamic simulations, binding free energy calculations, and binding pose metadynamics. We identified Elvitegravir as a potential inhibitor of MPXV virus using our comprehensive pipeline.
KW - Deep learning
KW - DeepRepurpose
KW - Double-stranded DNA
KW - Metadynamics
KW - Molecular docking and binding pose
KW - Monkeypox virus
UR - https://www.scopus.com/pages/publications/85151307173
U2 - 10.1016/j.jiph.2023.03.007
DO - 10.1016/j.jiph.2023.03.007
M3 - Article
C2 - 36966703
AN - SCOPUS:85151307173
SN - 1876-0341
VL - 16
SP - 799
EP - 807
JO - Journal of Infection and Public Health
JF - Journal of Infection and Public Health
IS - 5
ER -