Institute of Medical Science and Technology, National Sun Yat-sen University, Kaohsiung 804201, Taiwan.
Rapid Screening Research Center for Toxicology and Biomedicine, National Sun Yat-sen University, Kaohsiung 804201, Taiwan.
Cells. 2022 Jun 14;11(12):1924. doi: 10.3390/cells11121924.
The new coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus (SARS-CoV-2) has been reported and spread globally. There is an urgent need to take urgent measures to treat and prevent further infection of this virus. Here, we use virtual drug screening to establish pharmacophore groups and analyze the ACE2 binding site of the spike protein with the ZINC drug database and DrugBank database by molecular docking and molecular dynamics simulations. Screening results showed that Venetoclax, a treatment drug for chronic lymphocytic leukemia, has a potential ability to bind to the spike protein of SARS-CoV-2. In addition, our in vitro study found that Venetoclax degraded the expression of the spike protein of SARS-CoV-2 through amino acids Q493 and S494 and blocked the interaction with the ACE2 receptor. Our results suggest that Venetoclax is a candidate for clinical prevention and treatment and deserves further research.
新型冠状病毒病 2019(COVID-19)由严重急性呼吸系统综合症冠状病毒(SARS-CoV-2)引起,已在全球范围内被报告和传播。目前急需采取紧急措施来治疗和预防该病毒的进一步感染。在这里,我们使用虚拟药物筛选技术,通过分子对接和分子动力学模拟,从 ZINC 药物数据库和 DrugBank 数据库中建立药效团组并分析尖峰蛋白的 ACE2 结合位点。筛选结果表明,慢性淋巴细胞白血病治疗药物 Venetoclax 具有与 SARS-CoV-2 尖峰蛋白结合的潜在能力。此外,我们的体外研究发现 Venetoclax 通过氨基酸 Q493 和 S494 降解 SARS-CoV-2 尖峰蛋白的表达,并阻断与 ACE2 受体的相互作用。我们的研究结果表明 Venetoclax 是一种临床预防和治疗的候选药物,值得进一步研究。