Genomics Research Center, Academia Sinica, Taipei 115, Taiwan.
School of Pharmacy, National Taiwan University, Taipei 110, Taiwan.
Proc Natl Acad Sci U S A. 2021 Feb 2;118(5). doi: 10.1073/pnas.2021579118.
The outbreak of COVID-19 caused by SARS-CoV-2 has resulted in more than 50 million confirmed cases and over 1 million deaths worldwide as of November 2020. Currently, there are no effective antivirals approved by the Food and Drug Administration to contain this pandemic except the antiviral agent remdesivir. In addition, the trimeric spike protein on the viral surface is highly glycosylated and almost 200,000 variants with mutations at more than 1,000 positions in its 1,273 amino acid sequence were reported, posing a major challenge in the development of antibodies and vaccines. It is therefore urgently needed to have alternative and timely treatments for the disease. In this study, we used a cell-based infection assay to screen more than 3,000 agents used in humans and animals, including 2,855 small molecules and 190 traditional herbal medicines, and identified 15 active small molecules in concentrations ranging from 0.1 nM to 50 μM. Two enzymatic assays, along with molecular modeling, were then developed to confirm those targeting the virus 3CL protease and the RNA-dependent RNA polymerase. Several water extracts of herbal medicines were active in the cell-based assay and could be further developed as plant-derived anti-SARS-CoV-2 agents. Some of the active compounds identified in the screen were further tested in vivo, and it was found that mefloquine, nelfinavir, and extracts of (RF3), , and were effective in a challenge study using hamsters as disease model.
截至 2020 年 11 月,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 大流行已导致全球 5000 多万例确诊病例和超过 100 万人死亡。目前,除了抗病毒药物瑞德西韦之外,美国食品和药物管理局尚未批准任何有效的抗病毒药物来控制这种大流行。此外,病毒表面的三聚体刺突蛋白高度糖基化,在其 1273 个氨基酸序列中超过 1000 个位置发生突变的变体超过 20 万种,这给抗体和疫苗的开发带来了重大挑战。因此,迫切需要为这种疾病提供替代和及时的治疗方法。在这项研究中,我们使用基于细胞的感染测定法筛选了 3000 多种用于人类和动物的药物,包括 2855 种小分子和 190 种传统草药,发现了 15 种浓度在 0.1 nM 至 50 μM 之间的有效小分子。然后,我们开发了两种酶测定法以及分子建模,以确认这些药物的靶标是病毒 3CL 蛋白酶和 RNA 依赖性 RNA 聚合酶。几种草药的水提取物在基于细胞的测定中具有活性,可进一步开发为植物源性抗 SARS-CoV-2 药物。在体内进一步测试了筛选出的一些活性化合物,发现甲氟喹、奈非那韦和 的水提取物、 、 在使用仓鼠作为疾病模型的攻毒研究中有效。