Ensemble-Based Virtual Screening Led to the Discovery of Novel Lead Molecules as Potential NMBAs
Yi Zhang, Gonghui Ge, Xiangyang Xu, Jinhui Wu

TL;DR
This study used virtual screening to find new potential neuromuscular blocking agents that could help with muscle relaxation during anesthesia.
Contribution
The study introduces an ensemble-based virtual screening approach to discover novel lead molecules for NMBAs.
Findings
Hit compounds showed better docking scores than d-tubocurarine.
ZINC257459695 stably binds to nAChRs and interacts with key residue Asp165.
ADMET properties of hit compounds were evaluated for pharmacokinetic suitability.
Abstract
Neuromuscular blocking agents (NMBAs) are routinely used during anesthesia to relax skeletal muscle. Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels; NMBAs can induce muscle paralysis by preventing the neurotransmitter acetylcholine (ACh) from binding to nAChRs situated on the postsynaptic membranes. Despite widespread efforts, it is still a great challenge to find new NMBAs since the introduction of cisatracurium in 1995. In this work, an effective ensemble-based virtual screening method, including molecular property filters, 3D pharmacophore model, and molecular docking, was applied to discover potential NMBAs from the ZINC15 database. The results showed that screened hit compounds had better docking scores than the reference compound d-tubocurarine. In order to further investigate the binding modes between the hit compounds and nAChRs at simulated…
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Taxonomy
TopicsNicotinic Acetylcholine Receptors Study · Computational Drug Discovery Methods · Receptor Mechanisms and Signaling
