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对抗新型冠状病毒的中草药化合物:葛根素和槲皮素可削弱病毒S蛋白与ACE2受体的结合。

Chinese herbal compounds against SARS-CoV-2: Puerarin and quercetin impair the binding of viral S-protein to ACE2 receptor.

作者信息

Pan Boyu, Fang Senbiao, Zhang Ju, Pan Ya, Liu Han, Wang Yun, Li Min, Liu Liren

机构信息

Department of Gastrointestinal Cancer Biology, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin's Clinical Research Center for Cancer, Tianjin 300060, China.

School of Computer Science and Engineering, Central South University, Changsha 410006, Hunan, China.

出版信息

Comput Struct Biotechnol J. 2020;18:3518-3527. doi: 10.1016/j.csbj.2020.11.010. Epub 2020 Nov 11.

Abstract

The outbreak of COVID-19 raises an urgent need for the therapeutics to contain the emerging pandemic. However, no effective treatment has been found for SARS-CoV-2 infection to date. Here, we identified puerarin (PubChem CID: 5281807), quercetin (PubChem CID: 5280343) and kaempferol (PubChem CID: 5280863) as potential compounds with binding activity to ACE2 by using Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP). Molecular docking analysis showed that puerarin and quercetin exhibit good binding affinity to ACE2, which was validated by surface plasmon resonance (SPR) assay. Furthermore, SPR-based competition assay revealed that puerarin and quercetin could significantly affect the binding of viral S-protein to ACE2 receptor. Notably, quercetin could also bind to the RBD domain of S-protein, suggesting not only a receptor blocking, but also a virus neutralizing effect of quercetin on SARS-CoV-2. The results from network pharmacology and bioinformatics analysis support a view that quercetin is involved in host immunomodulation, which further renders it a promising candidate against COVID-19. Moreover, given that puerarin is already an existing drug, results from this study not only provide insight into its action mechanism, but also propose a prompt application of it on COVID-19 patients for assessing its clinical feasibility.

摘要

新型冠状病毒肺炎(COVID-19)的爆发引发了对控制这一新兴大流行疾病的治疗方法的迫切需求。然而,迄今为止尚未找到针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的有效治疗方法。在此,我们通过使用中药系统药理学数据库及分析平台(TCMSP),确定了葛根素(PubChem CID:5281807)、槲皮素(PubChem CID:5280343)和山奈酚(PubChem CID:5280863)为具有与血管紧张素转换酶2(ACE2)结合活性的潜在化合物。分子对接分析表明,葛根素和槲皮素对ACE2表现出良好的结合亲和力,这通过表面等离子体共振(SPR)测定得到了验证。此外,基于SPR的竞争测定表明,葛根素和槲皮素可显著影响病毒刺突蛋白(S蛋白)与ACE2受体的结合。值得注意的是,槲皮素还可与S蛋白的受体结合域(RBD)结合,这表明槲皮素对SARS-CoV-2不仅具有受体阻断作用,还具有病毒中和作用。网络药理学和生物信息学分析结果支持这样一种观点,即槲皮素参与宿主免疫调节,这进一步使其成为对抗COVID-19的有前景的候选药物。此外,鉴于葛根素已是一种现有药物,本研究结果不仅深入了解了其作用机制,还提出了将其迅速应用于COVID-19患者以评估其临床可行性的建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f1b/7700970/f3bacf8f5f47/ga1.jpg

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