Chemistry of Colombian Plants, Institute of Chemistry, Faculty of Exact and Natural Sciences, University of Antioquia-UdeA, Medellin, Colombia.
Academic Department of Pharmacology Bromatology and Toxicology,Faculty of Pharmacy and Biochemistry, Universidad Nacional Mayor de San Marcos, Lima, Peru.
J Biomol Struct Dyn. 2022 Mar;40(5):2227-2243. doi: 10.1080/07391102.2020.1837676. Epub 2020 Oct 29.
COVID-19 is a novel severe acute respiratory syndrome coronavirus. Currently, there is no effective treatment and vaccines seem to be the solution in the future. Virtual screening of potential drugs against the S protein of severe acute respiratory syndrome corona virus 2 (SARS-CoV-2) has provided small molecular compounds with a high binding affinity. Unfortunately, most of these drugs do not attach with the binding interface of the receptor-binding domain (RBD)-angiotensin-converting enzyme-2 (ACE-2) complex in host cells. Molecular modeling was carried out to evaluate the potential antiviral properties of the components of the medicinal herb (cat's claw) focusing on the binding interface of the RBD-ACE-2 and the viral spike protein. The in silico approach starts with protein-ligand docking of 26 Cat's claw key components followed by molecular dynamics simulations and re-docked calculations. Finally, we carried out drug-likeness calculations for the most qualified cat's claw components. The structural bioinformatics approaches led to the identification of several bioactive compounds of with potential therapeutic effect by dual strong interaction with interface of the RBD-ACE-2 and the ACE-2 binding site on SARS-CoV-2 RBD viral spike. In addition, in silico drug-likeness indices for these components were calculated and showed good predicted therapeutic profiles of these phytochemicals found in (cat's claw). Our findings suggest the potential effectiveness of cat's claw as complementary and/or alternative medicine for COVID-19 treatment.Communicated by Ramaswamy H. Sarma.
新型冠状病毒肺炎(COVID-19)是一种新型的严重急性呼吸系统综合征冠状病毒。目前尚无有效的治疗方法,疫苗似乎是未来的解决方案。针对严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)S 蛋白的虚拟筛选已经为具有高结合亲和力的小分子化合物提供了可能。不幸的是,这些药物中的大多数都不能与宿主细胞中受体结合域(RBD)-血管紧张素转换酶 2(ACE-2)复合物的结合界面结合。进行了分子建模,以评估药用植物(猫爪草)成分的潜在抗病毒特性,重点是 RBD-ACE-2 和病毒刺突蛋白的结合界面。基于结构的计算方法从 26 种猫爪草关键成分的蛋白配体对接开始,然后进行分子动力学模拟和重新对接计算。最后,我们对最合格的猫爪草成分进行了药物相似性计算。结构生物信息学方法导致鉴定了几种具有潜在治疗作用的生物活性化合物,它们通过与 RBD-ACE-2 的界面和 SARS-CoV-2 RBD 病毒刺突上的 ACE-2 结合位点的双重强相互作用。此外,还计算了这些成分的基于计算机的药物相似性指数,并显示出这些在猫爪草中发现的植物化学物质具有良好的预测治疗特征。我们的研究结果表明,猫爪草作为 COVID-19 治疗的补充和/或替代药物具有潜在的有效性。由 Ramaswamy H. Sarma 交流。