Nayak Digant, Dos Santos Bury Priscila, Drag Marcin, Nijkerk Alfred N, El Oualid Farid, Olsen Shaun K
Department of Biochemistry & Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Department of Chemical Biology and Bioimaging, Wroclaw University of Science and Technology, Wroclaw, Poland.
Methods Mol Biol. 2023;2591:171-188. doi: 10.1007/978-1-0716-2803-4_11.
Both severe acute respiratory syndrome coronavirus 1 and 2 (SARS-CoV-1 and SARS-CoV-2) encode a papain-like protease (PLpro), which plays a vital role in viral propagation. PLpro accomplishes this function by processing the viral polyproteins essential for viral replication and removing the small proteins, ubiquitin and ISG15 from the host's key immune signaling proteins, thereby preventing the host's innate immune response. Although PLpro from both SARS-CoV-1 and SARS-CoV-2 are structurally highly similar (83% sequence identity), they exhibit functional variability. Hence, to further elucidate the mechanism and aid in drug discovery efforts, the biochemical and kinetic characterization of PLpro is needed. This chapter describes step-by-step experimental procedures for evaluating PLpro activity in vitro using activity-based probes (ABPs) along with fluorescence-based substrates. Herein we describe a step-by-step experimental procedure to assess the activity of PLpro in vitro using a suite of activity-based probes (ABPs) and fluorescent substrates and how they can be applied as fast and yet sensitive methods to calculate kinetic parameters.
严重急性呼吸综合征冠状病毒1和2(SARS-CoV-1和SARS-CoV-2)均编码一种木瓜样蛋白酶(PLpro),该酶在病毒传播中起着至关重要的作用。PLpro通过加工病毒复制所必需的病毒多聚蛋白并从宿主关键免疫信号蛋白中去除小蛋白泛素和ISG15来实现这一功能,从而阻止宿主的先天免疫反应。尽管来自SARS-CoV-1和SARS-CoV-2的PLpro在结构上高度相似(序列同一性为83%),但它们表现出功能变异性。因此,为了进一步阐明其机制并助力药物研发工作,需要对PLpro进行生化和动力学表征。本章介绍了使用基于活性的探针(ABP)以及基于荧光的底物在体外评估PLpro活性的逐步实验程序。在此,我们描述了一个逐步实验程序,用于使用一套基于活性的探针(ABP)和荧光底物在体外评估PLpro的活性,以及如何将它们用作快速且灵敏的方法来计算动力学参数。