Department of Microbiology, University of Seville, Seville, Spain.
Methods Mol Biol. 2024;2751:165-178. doi: 10.1007/978-1-0716-3617-6_11.
Eukaryote-interacting bacteria have developed along the evolution of an arsenal of tools to interact with potential hosts and to evade their defensive responses. Among these tools, the effector proteins are gaining a special importance due to the high diversity of molecular actions that they play in the host cell, with the final aim of taking the control over the cell. Bacteria inject these effectors into the cytosol of the host cells through distinct ways, as the type III secretion system. The study of the effectors' molecular roles inside the host cell is challenging, due in part to the lack of traceability of such proteins once they are delivered by the bacteria. Here, we describe in depth a methodology that combines the increase of the bacterial effector concentration by protein expression systems with the use of heterologous hosts to facilitate the visualization of the subcellular targeting of the effector inside the host cell by fluorescence microscopy.
真核生物相互作用的细菌在与潜在宿主相互作用并逃避其防御反应的过程中,发展了一系列工具。在这些工具中,由于效应蛋白在宿主细胞中发挥的分子作用具有高度多样性,因此它们越来越受到重视,其最终目的是控制细胞。细菌通过不同的方式,如 III 型分泌系统,将这些效应蛋白注入宿主细胞的细胞质中。由于细菌输送后这些蛋白缺乏可追踪性,因此研究效应蛋白在宿主细胞内的分子作用具有一定的挑战性。在这里,我们详细描述了一种结合蛋白表达系统增加细菌效应蛋白浓度与利用异源宿主相结合的方法,通过荧光显微镜方便地可视化效应蛋白在宿主细胞内的亚细胞靶向。