Institut Pasteur, Université Paris Cité, Innovation Lab: Vaccines, Paris, France.
Institut de recherche biomédicale des armées, Immunopathologie, Bretigny-sur-Orge, France.
Methods Mol Biol. 2024;2808:89-103. doi: 10.1007/978-1-0716-3870-5_7.
The study of virus-host interactions is essential to achieve a comprehensive understanding of the viral replication process. The commonly used methods are yeast two-hybrid approach and transient expression of a single tagged viral protein in host cells followed by affinity purification of interacting cellular proteins and mass spectrometry analysis (AP-MS). However, by these approaches, virus-host protein-protein interactions are detected in the absence of a real infection, not always correctly compartmentalized, and for the yeast two-hybrid approach performed in a heterologous system. Thus, some of the detected protein-protein interactions may be artificial. Here we describe a new strategy based on recombinant viruses expressing tagged viral proteins to capture both direct and indirect protein partners during the infection (AP-MS in viral context). This way, virus-host protein-protein interacting co-complexes can be purified directly from infected cells for further characterization.
病毒-宿主相互作用的研究对于全面了解病毒复制过程至关重要。常用的方法是酵母双杂交方法和瞬时表达单个标记的病毒蛋白在宿主细胞中,然后通过亲和纯化相互作用的细胞蛋白和质谱分析(AP-MS)。然而,通过这些方法,病毒-宿主蛋白-蛋白相互作用是在没有真正感染的情况下检测到的,并不总是正确地分隔开,并且对于在异源系统中进行的酵母双杂交方法也是如此。因此,一些检测到的蛋白-蛋白相互作用可能是人为的。在这里,我们描述了一种新的策略,基于表达标记病毒蛋白的重组病毒,在感染过程中捕获直接和间接的蛋白伙伴(病毒背景下的 AP-MS)。通过这种方式,可以直接从感染细胞中纯化病毒-宿主蛋白-蛋白相互作用的复合物,以进行进一步的表征。