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强效植物化学物质荭草素作为严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白和宿主细胞受体葡萄糖调节蛋白78(GRP78)结合抑制剂的验证

validation of potent phytochemical orientin as inhibitor of SARS-CoV-2 spike and host cell receptor GRP78 binding.

作者信息

Bhowmik Arijit, Biswas Souradeep, Hajra Subhadip, Saha Prosenjit

机构信息

Department of Cancer Chemoprevention, Chittaranjan National Cancer Institute (CNCI), Kolkata, West Bengal, India.

出版信息

Heliyon. 2021 Jan;7(1):e05923. doi: 10.1016/j.heliyon.2021.e05923. Epub 2021 Jan 11.

Abstract

The present wellbeing worry to the whole world is the outbreak of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), also called COVID-19. This global health crisis first appeared in Wuhan, China around December 2019 and due to its extremely contagious nature it had spread to almost 187 countries. Still now no effective method of treatment or vaccine is developed for controlling the disease. Therefore, the sole obliging strategy is to take precautionary measures by repurposing drugs from the pre-existing library of therapeutically potent molecules. In this situation of pandemic this repurposing technique may save the labour-intensive and tiresome process of new drug development. Orientin is a natural flavonoid with several beneficial effects. This phytochemical can be isolated from different plants like tulsi or holy basil, black bamboo, passion flowers etc. It's antiviral, anti-inflammation, vasodilatation, cardioprotective, radioprotective, neuroprotective, anticarcinogenic and antinociceptive effects are already established. In this research, it is intriguing to find out whether this molecule can interfere the interaction of SARS-CoV-2 spike glycoprotein and their host receptor GRP78. Our docking and molecular dynamics simulation results indicate the binding of Orientin in the overlapping residues of GRP78 binding region of SARS-CoV-2 spike model and SARS-CoV-2 spike model binding region of GRP78 substrate-binding domain. Therefore, the results included in this research work provide a strong possibility of using Orientin as a promising precautionary or therapeutic measure for COVID-19.

摘要

目前,全球面临的健康担忧是严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的爆发,该病毒也被称为COVID-19。这场全球健康危机于2019年12月左右首次在中国武汉出现,由于其极强的传染性,已蔓延至近187个国家。目前仍未开发出有效的治疗方法或疫苗来控制这种疾病。因此,唯一可行的策略是通过重新利用现有治疗有效分子库中的药物来采取预防措施。在这种大流行的情况下,这种重新利用技术可以省去新药开发中劳动强度大且繁琐的过程。荭草素是一种具有多种有益作用的天然黄酮类化合物。这种植物化学物质可以从不同的植物中分离出来,如罗勒或圣罗勒、黑竹、西番莲等。其抗病毒、抗炎、血管舒张、心脏保护、辐射保护、神经保护、抗癌和抗伤害感受作用已经得到证实。在这项研究中,探究这种分子是否能干扰SARS-CoV-2刺突糖蛋白与其宿主受体GRP78的相互作用很有意思。我们的对接和分子动力学模拟结果表明,荭草素在SARS-CoV-2刺突模型的GRP78结合区域和GRP78底物结合域的SARS-CoV-2刺突模型结合区域的重叠残基中结合。因此,本研究工作所得结果提供了将荭草素用作COVID-19有前景的预防或治疗措施的很大可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79e1/7820743/0dbb9713ce38/gr1.jpg

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