Division of Pre-clinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH), Rockville, MD 20850, USA.
Division of Pre-clinical Innovation, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH), Rockville, MD 20850, USA.
Drug Discov Today. 2021 Oct;26(10):2439-2444. doi: 10.1016/j.drudis.2021.05.012. Epub 2021 May 25.
In response to the ongoing coronavirus disease 2019 (COVID-19) pandemic, a panel of assays has been developed and applied to screen collections of approved and investigational drugs for anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) activity in a quantitative high-throughput screening (qHTS) format. In this review, we applied data-driven approaches to evaluate the ability of each assay to identify potential anti-SARS-CoV-2 leads. Multitarget assays were found to show advantages in terms of accuracy and efficiency over single-target assays, whereas target-specific assays were more suitable for investigating compound mechanisms of action. Moreover, strict filtering with counter screens might be more detrimental than beneficial in identifying true positives. Thus, developing novel HTS assays acting simultaneously against multiple targets in the SARS-CoV-2 life cycle will benefit anti-COVID-19 drug discovery.
针对持续的 2019 年冠状病毒病(COVID-19)大流行,已经开发并应用了一组检测方法,以在定量高通量筛选(qHTS)格式下筛选已批准和正在研究的药物,以筛选抗严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的活性。在这篇综述中,我们应用数据驱动的方法来评估每种检测方法识别潜在抗 SARS-CoV-2 先导化合物的能力。与单靶标检测方法相比,多靶标检测方法在准确性和效率方面具有优势,而靶标特异性检测方法更适合研究化合物的作用机制。此外,使用反筛进行严格筛选可能弊大于利,不利于识别真正的阳性结果。因此,开发针对 SARS-CoV-2 生命周期中多个靶标同时作用的新型高通量检测方法将有利于抗 COVID-19 药物的发现。