芦丁通过抑制RNA依赖性RNA聚合酶抗SARS-CoV-2潜力的硅内和体外研究

IF 3.5 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ahmed M Metwaly, Esmail M El-Fakharany, Aisha A Alsfouk, Ibrahim M Ibrahim, Eslam B Elkaeed, Ibrahim H Eissa
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引用次数: 0

摘要

为了寻找有效的SARS-CoV-2抑制剂,我们对芦丁对9种SARS-CoV-2蛋白的结合和抑制效果进行了广泛的研究。方法:我们分析的第一步涉及与这些蛋白质相关的共结晶配体之间的结构相似性的全面检查。芦丁与SARS-CoV-2 RNA依赖性RNA聚合酶(RdRp)的配体Remdesivir在结构上有很大的相似性。这种相似性通过柔性对齐研究得到了验证。涉及叠加的分子对接研究揭示了芦丁和Remdesivir在RdRp活性位点内的结合模式有显著的相似性。200 ns分子动力学(MD)模拟证实rdrp -芦丁复合物比RdRp-Remdesivir复合物更稳定。结果:MM-GBSA实验表明,芦丁的结合能为-7.76 kcal/mol,明显低于雷姆德西韦的-2.15 kcal/mol。这表明RdRp-Rutin结合更加稳健和稳定,PLIP和ProLIF研究有助于阐明3D结合相互作用,并证实了MD模拟中看到的稳定结合。PCAT为rdrp -芦丁复合物的动态行为提供了更多的见解。体外实验表明,芦丁对RdRp具有较强的抑制作用,IC50为60.09 nM,显著优于瑞德西韦的24.56µM。值得注意的是,芦丁对SARS-CoV-2的体外IC50为0.598µg/ml,优于瑞德西韦(12.47µg/ml)。结论:与瑞德西韦(Remdesivir)相比,芦丁(SI: 1078)的选择性指数值突出了芦丁的特殊安全边际(SI: 5.8)。总之,我们的综合分析表明,芦丁作为一种有效的SARS-CoV-2 RdRp抑制剂具有很大的潜力,为开发有效的COVID-19治疗方法提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrated in Silico and in Vitro Studies of Rutin's Potential against SARS-CoV-2 through the Inhibition of the RNA-dependent RNA Polymerase.

Introduction: In our quest to identify potent inhibitors against SARS-CoV-2, an extensive investigation was conducted for the binding and inhibitory efficacy of Rutin against nine SARS-CoV-2 proteins.

Method: The first step of our analysis involved a comprehensive examination of structural similarity among the co-crystallized ligands associated with those proteins. A substantial structural similarity was observed between Rutin and Remdesivir, the ligand of the SARS-CoV-2 RNA-dependent RNA polymerase (RdRp). This similarity was validated through a flexible alignment study. Molecular docking studies, involving superimposition, revealed a notable resemblance in the mode of binding between Rutin and Remdesivir inside the active site of the RdRp. A 200 ns molecular dynamics (MD) simulation confirmed that the RdRp-Rutin complex is more stable than the RdRp-Remdesivir complex.

Result: The MM-GBSA studies showed that Rutin had much more favorable binding energies, with a significantly lower value of -7.76 kcal/mol compared to Remdesivir's -2.15 kcal/mol. This indicates that the RdRp-Rutin binding is more robust and stable PLIP and ProLIF studies helped clarify the 3D binding interactions and confirmed the stable binding seen in MD simulations. PCAT gave more insights into the dynamic behavior of the RdRp-Rutin complex. in vitro tests showed that Rutin has a strong inhibitory effect on RdRp with an IC50 of 60.09 nM, significantly outperforming Remdesivir, which has an IC50 of 24.56 µM. Remarkably, against SARS-CoV-2, Rutin showed a superior in vitro IC50 of 0.598 µg/ml compared to Remdesivir (12.47 µg/ml).

Conclusion: The values of the selectivity index underscored the exceptional margin of safety of Rutin (SI: 1078) compared to Remdesivir (SI: 5.8). In conclusion, our comprehensive analysis indicates Rutin's promising potential as a potent SARS-CoV-2 RdRp inhibitor, providing a valuable insight for developing an effective COVID-19 treatment.

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来源期刊
Current medicinal chemistry
Current medicinal chemistry 医学-生化与分子生物学
CiteScore
8.60
自引率
2.40%
发文量
468
审稿时长
3 months
期刊介绍: Aims & Scope Current Medicinal Chemistry covers all the latest and outstanding developments in medicinal chemistry and rational drug design. Each issue contains a series of timely in-depth reviews and guest edited thematic issues written by leaders in the field covering a range of the current topics in medicinal chemistry. The journal also publishes reviews on recent patents. Current Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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