Hasan Tarique N, Naqvi Syed S, Rehman Mati Ur, Ullah Rooh, Ammad Muhammad, Arshad Narmeen, Ain Qurat Ul, Perween Shabana, Hussain Arif
Pure Health Laboratory, Mafraq Hospital, Abu Dhabi, United Arab Emirates.
School of Life Sciences, Manipal Academy of Higher Education, Dubai, United Arab Emirates.
Narra J. 2023 Apr;3(1):e98. doi: 10.52225/narra.v3i1.98. Epub 2023 Feb 13.
The available drugs against coronavirus disease 2019 (COVOD-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), are limited. This study aimed to identify ginger-derived compounds that might neutralize SARS-CoV-2 and prevent its entry into host cells. Ring compounds of ginger were screened against spike (S) protein of alpha, beta, gamma, and delta variants of SARS-CoV-2. The S protein FASTA sequence was retrieved from Global Initiative on Sharing Avian Influenza Data (GISAID) and converted into ".pdb" format using Open Babel tool. A total of 306 compounds were identified from ginger through food and phyto-databases. Out of those, 38 ring compounds were subjected to docking analysis using CB Dock online program which implies AutoDock Vina for docking. The Vina score was recorded, which reflects the affinity between ligands and receptors. Further, the Protein Ligand Interaction Profiler (PLIP) program for detecting the type of interaction between ligand-receptor was used. SwissADME was used to compute druglikeness parameters and pharmacokinetics characteristics. Furthermore, energy minimization was performed by using Swiss PDB Viewer (SPDBV) and energy after minimization was recorded. Molecular dynamic simulation was performed to find the stability of protein-ligand complex and root-mean- square deviation (RMSD) as well as root-mean-square fluctuation (RMSF) were calculated and recorded by using myPresto v5.0. Our study suggested that 17 out of 38 ring compounds of ginger were very likely to bind the S protein of SARS-CoV-2. Seventeen out of 38 ring compounds showed high affinity of binding with S protein of alpha, beta, gamma, and delta variants of SARS-CoV-2. The RMSD showed the stability of the complex was parallel to the S protein monomer. These computer-aided predictions give an insight into the possibility of ginger ring compounds as potential anti-SARS-CoV-2 worthy of in vitro investigations.
用于对抗由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019冠状病毒病(COVID-19)的现有药物有限。本研究旨在鉴定可能中和SARS-CoV-2并阻止其进入宿主细胞的姜衍生化合物。针对SARS-CoV-2的α、β、γ和δ变体的刺突(S)蛋白筛选姜的环状化合物。S蛋白的FASTA序列从全球共享禽流感数据倡议组织(GISAID)获取,并使用Open Babel工具转换为“pdb”格式。通过食品和植物数据库从姜中总共鉴定出306种化合物。其中,38种环状化合物使用CB Dock在线程序进行对接分析,该程序使用AutoDock Vina进行对接。记录Vina分数,其反映配体与受体之间的亲和力。此外,使用蛋白质配体相互作用分析器(PLIP)程序检测配体 - 受体之间的相互作用类型。使用SwissADME计算类药性质参数和药代动力学特征。此外,使用瑞士PDB查看器(SPDBV)进行能量最小化,并记录最小化后的能量。进行分子动力学模拟以发现蛋白质 - 配体复合物的稳定性,并使用myPresto v5.0计算和记录均方根偏差(RMSD)以及均方根波动(RMSF)。我们的研究表明,姜的38种环状化合物中有17种非常可能与SARS-CoV-2的S蛋白结合。38种环状化合物中有17种与SARS-CoV-2的α、β、γ和δ变体的S蛋白表现出高结合亲和力。RMSD表明复合物的稳定性与S蛋白单体平行。这些计算机辅助预测深入了解了姜环状化合物作为潜在抗SARS-CoV-2药物进行体外研究的可能性。