Wagner Nicole D, Price David A, Leung Daisy W
Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Department of Chemistry, Washington University in St. Louis, St. Louis, MO, USA.
Methods Mol Biol. 2025;2948:211-232. doi: 10.1007/978-1-0716-4666-3_14.
Human respiratory syncytial virus (RSV) encodes multifunctional viral proteins that form interactions with each other and with host proteins during different stages of the viral replication cycle to facilitate viral replication and pathogenesis. Biochemical and biophysical characterization of protein-protein interactions is important for validation and for providing insights into the regulatory mechanisms used by viral proteins during RSV infections. In this chapter, we describe a process that can be used to validate direct protein-protein interactions by in vitro pulldown assay and biophysical characterization using size-exclusion chromatography-multiangle light scattering (SEC-MALS) and hydrogen-deuterium exchange-mass spectrometry (HDX-MS).
人呼吸道合胞病毒(RSV)编码多功能病毒蛋白,这些蛋白在病毒复制周期的不同阶段相互之间以及与宿主蛋白形成相互作用,以促进病毒复制和发病机制。蛋白质-蛋白质相互作用的生化和生物物理特性对于验证以及深入了解RSV感染期间病毒蛋白所使用的调控机制非常重要。在本章中,我们描述了一个可用于通过体外下拉试验以及使用尺寸排阻色谱-多角度光散射(SEC-MALS)和氢-氘交换质谱(HDX-MS)进行生物物理特性分析来验证直接蛋白质-蛋白质相互作用的过程。