Rashmi Sahu, Rajan Mariappan, Awanish Kumar, Arun Kumar Mahapatra, S Rajagopala, Prashant Kumar Gupta
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引用次数: 0
摘要
猴痘是由猴痘病毒(MPXV)引起的病毒性人畜共患疾病,由于人与人之间的传播增加,最近已成为一项重大的全球健康威胁。截至2023年11月,麻疹疫情已影响到全球116个国家,共有92,783例确诊病例和171例报告死亡。由于可用的抗病毒选择有限,穿心莲等天然植物化合物已显示出其抗菌和抗病毒特性的希望。本研究通过计算方法探讨了金针藤抗猴痘病毒靶点的生物活性化合物的潜力。从蛋白数据库(Protein Data Bank, PDB)中获取蛋白结构4E90、8B07、8C9K、8IZT和8J8G,并使用Schrödinger Suite进行分子动力学模拟研究。此外,轨迹分析评估了配体-蛋白复合物的稳定性和结合亲和力。化合物穿心莲内酯、木犀草素和穿心莲内酯- a表现出很强的结合相互作用和稳定的蛋白质-配体复合物,以及良好的热力学特征,支持它们作为有希望的猴痘治疗候选者的潜力。补充信息:在线版本包含补充资料,提供地址为10.1007/s40203-025-00423-4。
Therapeutic potential of Andrographis paniculata against Monkeypox virus targets-a computational insight.
Monkeypox, a viral zoonotic disease caused by the monkeypox virus (MPXV), has recently become a significant global health threat due to increased human-to-human transmission. As of November 2023, the Mpox outbreak had impacted 116 countries worldwide, with a total of 92,783 confirmed cases and 171 reported deaths. With limited antiviral options available, natural plant-based compounds like Andrographis paniculata have shown promise for their antimicrobial and antiviral properties. This study explores the potential of bioactive compounds from A. paniculata against monkeypox viral targets through computational methods. Protein structures 4E90, 8B07, 8C9K, 8IZT and 8J8G were obtained from the Protein Data Bank (PDB), and molecular dynamic simulation studies were conducted using the Schrödinger Suite. Furthermore, the trajectory analysis assessed the stability and binding affinity of the ligand-protein complexes. The compounds andrographolide, luteolin, and andrographidin-A demonstrated strong binding interactions and stable protein-ligand complexes, along with favorable thermodynamic profiles, supporting their potential as promising therapeutic candidates for monkeypox treatment.
Supplementary information: The online version contains supplementary material available at 10.1007/s40203-025-00423-4.