Institute of Virology, Medical University of Innsbruck, Innsbruck, Austria.
These authors contributed equally to this work.
Curr Protoc. 2024 Nov;4(11):e70062. doi: 10.1002/cpz1.70062.
Protease inhibitors are among the most powerful antiviral drugs. They have been used successfully against viruses, such as the human immunodeficiency virus (HIV), hepatitis C virus (HCV) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Protease inhibitor screening tools are therefore important to identify inhibitors that have the potential to become antiviral drugs. In this article, we describe newly developed cell- and virus replicon-based platforms to screen inhibitors. We developed the methods presented here by genetically modifying vesicular stomatitis virus, a model virus from the family Rhabdoviridae. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol: M-On and -Off assay Alternate Protocol 1: Virus production with transient P- and L TransIT transfection Alternate Protocol 2: Virus production with transient P- and L CaPO transfection Alternate Protocol 3: Luciferase-based variation of the On assay Alternate Protocol 4: Screening assay with fluorescence-activated cell sorting readout Support Protocol: Performing kinetic measurements with Off assay.
蛋白酶抑制剂是最有效的抗病毒药物之一。它们已成功用于对抗病毒,如人类免疫缺陷病毒(HIV)、丙型肝炎病毒(HCV)和严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)。因此,蛋白酶抑制剂筛选工具对于鉴定具有成为抗病毒药物潜力的抑制剂非常重要。在本文中,我们描述了新开发的基于细胞和病毒复制子的筛选抑制剂的平台。我们通过遗传修饰水疱性口炎病毒(来自 Rhabdoviridae 科的一种模式病毒)来开发这里提出的方法。© 2024 作者。Wiley Periodicals LLC 出版的《当代协议》。基本方案:M-On 和 -Off 测定替代方案 1:使用瞬时 P-和 L TransIT 转染进行病毒生产替代方案 2:使用瞬时 P-和 L CaPO 转染进行病毒生产替代方案 3:基于荧光素酶的 On 测定变体替代方案 4:具有荧光激活细胞分选读数的筛选测定法支持方案:使用 Off 测定法进行动力学测量。