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贝塔冠状病毒病毒进入抑制剂的最新综述:从过去的发现中吸取教训,推进 COVID-19 药物发现。

An Updated Review on Betacoronavirus Viral Entry Inhibitors: Learning from Past Discoveries to Advance COVID-19 Drug Discovery.

机构信息

Department of Pharmacy, Faculty of Pharmacy, Al-Zaytoonah University of Jordan, P.O. Box 130 Amman, 11733, Jordan.

Department of Pharmaceutical Sciences, School of Pharmacy, University of Jordan, Amman 11942, Jordan.

出版信息

Curr Top Med Chem. 2021;21(7):571-596. doi: 10.2174/1568026621666210119111409.

Abstract

Even after one year of its first outbreak reported in China, the coronavirus disease 2019 (COVID-19) pandemic is still sweeping the World, causing serious infections and claiming more fatalities. COVID-19 is caused by the novel coronavirus SARS-CoV-2, which belongs to the genus Betacoronavirus (β-CoVs), which is of greatest clinical importance since it contains many other viruses that cause respiratory disease in humans, including OC43, HKU1, SARS-CoV, and MERS. The spike (S) glycoprotein of β-CoVs is a key virulence factor in determining disease pathogenesis and host tropism, and it also mediates virus binding to the host's receptors to allow viral entry into host cells, i.e., the first step in virus lifecycle. Viral entry inhibitors are considered promising putative drugs for COVID-19. Herein, we mined the biomedical literature for viral entry inhibitors of other coronaviruses, with special emphasis on β-CoVs entry inhibitors. We also outlined the structural features of SARS-CoV-2 S protein and how it differs from other β-CoVs to better understand the structural determinants of S protein binding to its human receptor (ACE2). This review highlighted several promising viral entry inhibitors as potential treatments for COVID-19.

摘要

即使在中国首次报告新冠病毒疾病(COVID-19)大流行一年后,它仍在席卷全球,导致严重感染并夺走更多生命。COVID-19 是由新型冠状病毒 SARS-CoV-2 引起的,该病毒属于β冠状病毒属(β-CoVs),具有最大的临床重要性,因为它包含许多其他可导致人类呼吸道疾病的病毒,包括 OC43、HKU1、SARS-CoV 和 MERS。β-CoVs 的刺突(S)糖蛋白是决定疾病发病机制和宿主嗜性的关键毒力因子,它还介导病毒与宿主受体的结合,从而允许病毒进入宿主细胞,即病毒生命周期的第一步。病毒进入抑制剂被认为是治疗 COVID-19 的有前途的潜在药物。本文从其他冠状病毒的生物医学文献中挖掘了病毒进入抑制剂,特别强调了β-CoVs 进入抑制剂。我们还概述了 SARS-CoV-2 S 蛋白的结构特征以及它与其他β-CoVs 的不同之处,以更好地了解 S 蛋白与人类受体(ACE2)结合的结构决定因素。这篇综述强调了几种有前途的病毒进入抑制剂作为 COVID-19 潜在治疗方法的潜力。

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