Gyebi Gideon Ampoma, Sabiu Saheed
Department of Biotechnology and Food Science, Faculty of Applied Sciences, Durban University of Technology, P.O. Box 1334, Durban 4000, South Africa.
Department of Biotechnology and Food Science, Faculty of Applied Sciences, Durban University of Technology, P.O. Box 1334, Durban 4000, South Africa.
Comput Biol Chem. 2025 Oct;118:108458. doi: 10.1016/j.compbiolchem.2025.108458. Epub 2025 Apr 11.
The growing global health threat of the monkeypox virus (MPXV) underscores the critical need for effective antiviral agents, since there are currently no therapeutics. The MPXV VP39, a methyltransferase, is essential for viral replication, hence a potential target for anti-MPXV drug candidates. Herein, a structure-based pharmacophore modelling and molecular docking approach was employed to screen natural compounds (NCs: 581,426) from the COCONUT database for potential inhibitors of MPXV VP39. After ranking of the docking scores, an ensemble-based docking of the top-ranked 20 NCs against multiple conformations obtained from ttcluster analysis of the molecular dynamics simulation trajectory of unbound MPXV VP39 further identified five leads with favourable interaction profiles, drug-likeness, ADMET properties, and synthetic features when compared to the reference standard (sinefungin). Further analysis of the thermodynamic stability of the resulting complexes of the leads over a 100-ns MD simulation period revealed varying degrees of thermodynamic stability while maintaining the structural integrity of MPXV VP39. Furthermore, the thermodynamic binding free energy calculation, while corroborating the docking analysis, identified CNP0297833 (-39.07 kcal/mol), CNP0371756 (-25.76 kcal/mol), and CNP0402319 (-19.26 kcal/mol) as the most promising candidates, with better modulatory effect against MPXV VP39 relative to sinefungin (-3.68 kcal/mol). These leads were stabilised with hydrophobic (Phe115, Val139, and Val116) and electrostatic (Glu46 and Asp138) interactions in different conformational clusters. In addition to the observed consistent interaction patterns, favourable binding energies, pharmacokinetics, ADMET, thermodynamic stability, and molecular orbital energies of these leads, the potential for optimisation for enhanced binding features for the active site of MPXV VP39 was elucidated. Further in vitro investigation to validate these findings is suggested to establish the putative leads as therapeutics targeting the replication phase of MPXV.
猴痘病毒(MPXV)对全球健康的威胁日益增加,凸显了对有效抗病毒药物的迫切需求,因为目前尚无治疗方法。MPXV的VP39是一种甲基转移酶,对病毒复制至关重要,因此是抗MPXV候选药物的潜在靶点。在此,采用基于结构的药效团建模和分子对接方法,从COCONUT数据库中筛选天然化合物(NCs:581,426种),寻找MPXV VP39的潜在抑制剂。对接分数排序后,将排名前20的NCs与从游离MPXV VP39分子动力学模拟轨迹的ttcluster分析获得的多个构象进行基于整体的对接,进一步确定了五个具有良好相互作用特征、类药性质、ADMET性质和合成特征的先导化合物,与参考标准品(西尼芬净)相比。在100 ns的分子动力学模拟期间对先导化合物形成的复合物的热力学稳定性进行进一步分析,结果显示在维持MPXV VP39结构完整性的同时,具有不同程度的热力学稳定性。此外,热力学结合自由能计算在证实对接分析的同时,确定CNP0297833(-39.07 kcal/mol)、CNP0371756(-25.76 kcal/mol)和CNP0402319(-19.26 kcal/mol)是最有前景的候选物,相对于西尼芬净(-3.68 kcal/mol),它们对MPXV VP39具有更好的调节作用。这些先导化合物在不同的构象簇中通过疏水相互作用(苯丙氨酸115、缬氨酸139和缬氨酸116)和静电相互作用(谷氨酸46和天冬氨酸138)得以稳定。除了观察到的这些先导化合物一致的相互作用模式、有利的结合能、药代动力学、ADMET、热力学稳定性和分子轨道能量外,还阐明了针对MPXV VP39活性位点优化增强结合特征的潜力。建议进一步进行体外研究以验证这些发现,从而将这些假定的先导化合物确立为针对MPXV复制阶段的治疗药物。