Faculty of Applied sciences and Biotechnology, Shoolini University of Biotechnology and Management Sciences, Bajhol, Himachal Pradesh, India.
Department of Pharmacology, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
J Biomol Struct Dyn. 2021 Nov;39(18):7017-7034. doi: 10.1080/07391102.2020.1804457. Epub 2020 Aug 27.
Currently, there is no specific treatment to cure COVID-19. Many medicinal plants have antiviral, antioxidant, antibacterial, antifungal, anticancer, wound healing etc. Therefore, the aim of the current study was to screen for potent inhibitors of N-terminal domain (NTD) of nucleocapsid phosphoprotein of SARS-CoV-2. The structure of NTD of RNA binding domain of nucleocapsid phosphoprotein of SARS coronavirus 2 was retrieved from the Protein Data Bank (PDB 6VYO) and the structures of 100 different phytocompounds were retrieved from Pubchem. The receptor protein and ligands were prepared using Schrodinger's Protein Preparation Wizard. Molecular docking was done by using the Schrodinger's maestro 12.0 software. Drug likeness and toxicity of active phytocompounds was predicted by using Swiss adme, admetSAR and protox II online servers. Molecular dynamic simulation of the best three protein- ligand complexes (alizarin, aloe-emodin and anthrarufin) was performed to study the interaction stability. We have identified three potential active sites (named as A, B, C) on receptor protein for efficient binding of the phytocompounds. We found that, among 100 phytocompounds, emodin, aloe-emodin, anthrarufin, alizarine, and dantron of showed good binding affinity at all the three active sites of RNA binding domain of nucleocapsid phosphoprotein of COVID-19.The binding energies of emodin, aloe-emodin, anthrarufin, alizarine, and dantron were -8.299, -8.508, -8.456, -8.441, and -8.322 Kcal mol respectively (site A), -7.714, -6.433, -6.354, -6.598, and -6.99 Kcal mol respectively (site B), and -8.299, 8.508, 8.538, 8.841, and 8.322 Kcal mol respectively (site C). All the active phytocompounds follows the drug likeness properties, non-carcinogenic, and non-toxic. Theses phytocompounds (alone or in combination) could be developed into effective therapy against COVID-19. From MD simulation data, we found that all three complexes of 6VYO with alizarin, aloe-emodin and anthrarufin were stable up to 50 ns. These phytocompounds can be tested further for or and used as a potential drug to cure SARS-CoV-2 infection.Communicated by Ramaswamy H. Sarma.
目前,尚无治愈 COVID-19 的特定方法。许多药用植物具有抗病毒、抗氧化、抗菌、抗真菌、抗癌、伤口愈合等功效。因此,本研究的目的是筛选 SARS-CoV-2 核衣壳磷蛋白 N 端结构域(NTD)的有效抑制剂。从蛋白质数据库(PDB 6VYO)中检索 SARS 冠状病毒核衣壳磷蛋白 RNA 结合域 NTD 的结构,并从 Pubchem 中检索 100 种不同植物化合物的结构。使用 Schrodinger 的 Protein Preparation Wizard 准备受体蛋白和配体。通过使用 Schrodinger 的 maestro 12.0 软件进行分子对接。使用 Swiss adme、admetSAR 和 protox II 在线服务器预测活性植物化合物的药物相似性和毒性。对最佳的三个蛋白-配体复合物(蒽醌、芦荟大黄素和蒽醌)进行分子动力学模拟,以研究相互作用的稳定性。我们已经确定了受体蛋白上三个有效的结合部位(分别命名为 A、B、C),用于有效结合植物化合物。我们发现,在 100 种植物化合物中,大黄素、芦荟大黄素、蒽醌、茜素和丹蒽酮在 COVID-19 核衣壳磷蛋白 RNA 结合域的所有三个活性部位均表现出良好的结合亲和力。大黄素、芦荟大黄素、蒽醌、茜素和丹蒽酮的结合能分别为-8.299、-8.508、-8.456、-8.441 和-8.322 Kcal mol(部位 A),-7.714、-6.433、-6.354、-6.598 和-6.99 Kcal mol(部位 B)和-8.299、8.508、8.538、8.841 和 8.322 Kcal mol(部位 C)。所有活性植物化合物均符合药物相似性特性、非致癌性和非毒性。这些植物化合物(单独或联合使用)可开发为有效治疗 COVID-19 的方法。从 MD 模拟数据来看,我们发现 6VYO 与茜素、芦荟大黄素和蒽醌的三个复合物均稳定达 50 ns。这些植物化合物可以进一步进行 或 测试,并用作治疗 SARS-CoV-2 感染的潜在药物。由 Ramaswamy H. Sarma 交流。