Ravi Deva Asirvatham, Hwang Du Hyeon, Mohan Prakash Ramachandran Loganathan, Kang Changkeun, Kim Euikyung
College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, Republic of Korea.
Institute of Animal Medicine, Gyeongsang National University, Jinju 52828, Republic of Korea.
Int J Mol Sci. 2024 Nov 26;25(23):12675. doi: 10.3390/ijms252312675.
Snakebite envenoming is a significant health threat, particularly in tropical regions, causing substantial morbidity and mortality. Traditional treatments, including antivenom therapy, have limitations and associated risks. This research aims to discover novel phytochemical antidotes for snakebites, specifically targeting the western diamondback rattlesnake () venom metalloproteinase Atrolysin. Utilizing pharmacoinformatic techniques such as molecular docking, high-throughput ligand screening, pharmacophore mapping, pharmacokinetic profiling, and molecular dynamics (MD) simulations, we analyzed phytochemicals from the Indian Medicinal Plants, Phytochemistry And Therapeutics (IMPPAT) database alongside well-known nine metalloproteinase inhibitors from the PubChem database. From an initial set of 17,967 compounds, 4708 unique compounds were identified for further study. These compounds were evaluated based on drug likeness, molecular descriptors, ADME properties, and toxicity profiles. Binding site predictions and molecular docking identified key interacting residues and binding energies, highlighting several promising compounds. Density functional theory (DFT) analysis provided insights into these compounds' electronic properties and stability. MD simulations assessed the dynamic stability of protein-ligand complexes using parameters such as RMSD, RMSF, the radius of gyration, and hydrogen bond interactions. This study identified top candidates, including CID5291, IMPHY001495, IMPHY014737, IMPHY008983, IMPHY008176, and IMPHY003833, based on their favorable binding energies, interaction forces, and structural stability. These findings suggest that the selected phytochemicals have the potential to serve as effective alternatives to traditional antivenom treatments, offering a promising avenue for further research and development in snakebite management.
蛇咬伤中毒是一项重大的健康威胁,尤其是在热带地区,会导致大量发病和死亡。包括抗蛇毒血清疗法在内的传统治疗方法存在局限性和相关风险。本研究旨在发现用于蛇咬伤的新型植物化学解毒剂,特别针对西部菱斑响尾蛇毒液金属蛋白酶Atrolysin。利用分子对接、高通量配体筛选、药效团映射、药代动力学分析和分子动力学(MD)模拟等药物信息学技术,我们分析了来自印度药用植物、植物化学与治疗学(IMPPAT)数据库的植物化学物质以及来自PubChem数据库的九种著名金属蛋白酶抑制剂。从最初的17967种化合物中,鉴定出4708种独特的化合物进行进一步研究。根据药物相似性、分子描述符、ADME性质和毒性概况对这些化合物进行了评估。结合位点预测和分子对接确定了关键的相互作用残基和结合能,突出了几种有前景的化合物。密度泛函理论(DFT)分析提供了对这些化合物电子性质和稳定性的见解。MD模拟使用均方根偏差(RMSD)、均方根波动(RMSF)、回转半径和氢键相互作用等参数评估了蛋白质-配体复合物的动态稳定性。基于其有利的结合能、相互作用力和结构稳定性,本研究确定了顶级候选物,包括CID5291、IMPHY001495、IMPHY014737、IMPHY008983、IMPHY008176和IMPHY003833。这些发现表明,所选的植物化学物质有可能作为传统抗蛇毒血清治疗的有效替代品,为蛇咬伤治疗的进一步研究和开发提供了一条有前景的途径。