1,7-Bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one inhibits SARS-CoV-2 by targeting the nucleocapsid protein

Yang Liu, Kuiru Sa, Wei-Na Xu, Yong-Quan Chen, Jing Liang, Peng Zou, Lixia Chen
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引用次数: 2

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has spread globally since 2020. The nucleocapsid (N) protein plays a crucial role in the life cycle of SARS-CoV-2. Here, we established a method to screen inhibitors of N protein by using microscale thermophoresis assays to obtain potential anti-SARS-CoV-2 agents. We identified 1,7-bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one (N-17, a diphenylheptane) as a compound with outstanding inhibitory activity. We further validated the binding of N-17 to the N-terminal domain of N protein (N-NTD) by using drug affinity responsive target stability assays. We evaluated the ability of N-17 to bind N protein and predicted the affinity of N-17 to the N-NTD with molecular docking and molecular dynamics simulation. N-17 exhibited excellent anti-viral activity against HCoV-OC43 and SARS-CoV-2, with EC50 values of 0.16 ± 0.01 μM and 0.17 ± 0.07 μM, respectively. Thus, we discovered a novel SARS-CoV-2 inhibitor targeting the N protein and validated its anti-viral activity in vitro. Our results may contribute to the development of promising therapeutic agents for COVID-19.
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1,7-二(4-羟基苯基)-1,4,6-庚三烯-3 -1通过靶向核衣壳蛋白抑制SARS-CoV-2
自2020年以来,严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)已在全球传播。核衣壳蛋白在SARS-CoV-2的生命周期中起着至关重要的作用。本研究建立了一种利用微尺度热泳法筛选N蛋白抑制剂的方法,以获得潜在的抗sars - cov -2药物。我们鉴定出1,7-二(4-羟基苯基)-1,4,6-庚烷-3 -1 (N-17,一种二苯庚烷)是一种具有显著抑制活性的化合物。我们进一步通过药物亲和反应性靶标稳定性试验验证了N-17与N蛋白N端结构域(N- ntd)的结合。通过分子对接和分子动力学模拟,评估了N-17与N蛋白的结合能力,并预测了N-17与N- ntd的亲和力。N-17对HCoV-OC43和SARS-CoV-2表现出良好的抗病毒活性,EC50值分别为0.16±0.01 μM和0.17±0.07 μM。因此,我们发现了一种新的靶向N蛋白的SARS-CoV-2抑制剂,并在体外验证了其抗病毒活性。我们的研究结果可能有助于开发有前景的COVID-19治疗药物。
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