National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, USA.
SLAS Discov. 2020 Dec;25(10):1141-1151. doi: 10.1177/2472555220942123. Epub 2020 Jul 13.
COVID-19 respiratory disease caused by the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has rapidly become a global health issue since it emerged in December 2019. While great global efforts are underway to develop vaccines and to discover or repurpose therapeutic agents for this disease, as of this writing only the nucleoside drug remdesivir has been approved under Emergency Use Authorization to treat COVID-19. The RNA-dependent RNA polymerase (RdRP), a viral enzyme for viral RNA replication in host cells, is one of the most intriguing and promising drug targets for SARS-CoV-2 drug development. Because RdRP is a viral enzyme with no host cell homologs, selective SARS-CoV-2 RdRP inhibitors can be developed that have improved potency and fewer off-target effects against human host proteins and thus are safer and more effective therapeutics for treating COVID-19. This review focuses on biochemical enzyme and cell-based assays for RdRPs that could be used in high-throughput screening to discover new and repurposed drugs against SARS-CoV-2.
自 2019 年 12 月出现以来,由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的 COVID-19 呼吸道疾病迅速成为一个全球性健康问题。虽然全球正在努力开发疫苗并发现或重新利用针对这种疾病的治疗药物,但截至目前,只有核苷药物瑞德西韦已获得紧急使用授权,可用于治疗 COVID-19。RNA 依赖性 RNA 聚合酶(RdRP)是一种在宿主细胞中复制病毒 RNA 的病毒酶,是 SARS-CoV-2 药物开发中最引人关注和最有前途的药物靶点之一。由于 RdRP 是一种没有宿主细胞同源物的病毒酶,因此可以开发出对 SARS-CoV-2 RdRP 具有更高选择性的抑制剂,这些抑制剂具有更高的效力和更少的针对人类宿主蛋白的脱靶效应,因此对于治疗 COVID-19 而言,它们更安全、更有效。本文综述了 RdRPs 的生化酶和基于细胞的测定方法,这些方法可用于高通量筛选,以发现针对 SARS-CoV-2 的新药和再利用药物。