Department of Physical Sciences and Mathematics, College of Arts and Sciences, University of the Philippines Manila, 1000, Manila, Philippines.
Department of Chemistry, De La Salle University, 2401 Taft Avenue, 0992, Manila, Philippines.
J Mol Model. 2022 Oct 7;28(11):345. doi: 10.1007/s00894-022-05334-1.
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, is a novel strain of coronavirus first reported in December 2019 which rapidly spread throughout the world and was subsequently declared a pandemic by the World Health Organization (WHO) in March 2020. Although vaccines, as well as treatments, have been rapidly developed and deployed, these are still spread thin, especially in the developing world. There is also a continuing threat of the emergence of mutated variants which may not be as responsive to available vaccines and drugs. Accessible and affordable sources of antiviral drugs against SARS-CoV-2 offer wider options for the clinical treatment of populations at risk for severe COVID-19. Using in silico methods, this study identified potential inhibitors against the SARS-CoV-2 main protease (Mpro), the protease directly responsible for the activation of the viral replication enzyme, from a consolidated database of 1516 Philippine natural products. Molecular docking experiments, along with in silico ADME predictions, determined top ligands from this database with the highest potential inhibitory effects against Mpro. Molecular dynamic trajectories of the apo and diosmetin-7-O-b-D-glucopyranoside (DG) in complex with the protein predicted potential mechanisms of action for the ligand-by separating the Cys145-His41 catalytic dyad and by influencing the protein network through key intra-signaling residues within the Mpro binding site. These findings show the inhibitory potential of DG against the SARS-CoV-2 Mpro, and further validation is recommended through in vitro or in vivo experimentation.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)是 COVID-19 的病原体,是一种新型冠状病毒,于 2019 年 12 月首次报告,迅速在全球传播,并随后于 2020 年 3 月被世界卫生组织(WHO)宣布为大流行。尽管疫苗和治疗方法已经迅速开发和部署,但这些仍然分布不均,尤其是在发展中国家。也存在突变变体不断出现的威胁,这些变体可能对现有疫苗和药物的反应不那么敏感。针对 SARS-CoV-2 的抗病毒药物的易得性和可负担性为面临严重 COVID-19 风险的人群的临床治疗提供了更广泛的选择。本研究使用计算机模拟方法,从 1516 种菲律宾天然产物的综合数据库中,确定了针对 SARS-CoV-2 主要蛋白酶(Mpro)的潜在抑制剂。分子对接实验,以及计算机预测的 ADME,确定了该数据库中与 Mpro 具有最高潜在抑制作用的顶级配体。apo 和二氢芫荽素-7-O-b-D-吡喃葡萄糖苷(DG)与蛋白复合物的分子动力学轨迹预测了配体的潜在作用机制,通过分离 Cys145-His41 催化二联体,并通过影响 Mpro 结合位点内的关键信号内残基来影响蛋白质网络。这些发现表明 DG 对 SARS-CoV-2 Mpro 的抑制潜力,建议通过体外或体内实验进一步验证。