Fritsch Verena Nadin, Hensel Michael
Abt. Mikrobiologie, Universität Osnabrück, Osnabrück, Germany.
Center for Cellular Nanoananalytics (CellNanOs), Universität Osnabrück, Osnabrück, Germany.
Bioessays. 2025 Apr;47(4):e202400188. doi: 10.1002/bies.202400188. Epub 2025 Mar 13.
Bacterial pathogens deliver effector proteins into host cells by deploying sophisticated secretion systems. This effector translocation during host-pathogen interactions is a prerequisite for the manipulation of host cells and organisms and is important for pathogenesis. Analyses of dynamics and kinetics of translocation, subcellular localization, and cellular targets of effector proteins lead to understanding the mode of action and function of effector proteins in host-pathogen interplay. This review provides an overview of biochemical and genetic tools that have been developed to study protein effector translocation qualitatively or quantitatively. After introducing the challenges of analyses of effector translocation during host-pathogen interaction, we describe various methods ranging from static visualization in fixed cells to dynamic live-cell imaging of effector protein translocation. We show the main findings enabled by the approaches, emphasize the advantages and limitations of the methods, describe recent approaches that allow real-time tracking of effector proteins in living cells on a single molecule level, and highlight open questions in the field to be addressed by application of new methods.
细菌病原体通过部署复杂的分泌系统将效应蛋白输送到宿主细胞中。在宿主-病原体相互作用过程中的这种效应蛋白易位是操纵宿主细胞和生物体的先决条件,对发病机制至关重要。对效应蛋白易位的动力学和动态过程、亚细胞定位以及细胞靶点的分析有助于理解效应蛋白在宿主-病原体相互作用中的作用方式和功能。本综述概述了为定性或定量研究蛋白效应蛋白易位而开发的生化和遗传工具。在介绍了宿主-病原体相互作用过程中效应蛋白易位分析的挑战之后,我们描述了从固定细胞中的静态可视化到效应蛋白易位的动态活细胞成像等各种方法。我们展示了这些方法所取得的主要发现,强调了这些方法的优点和局限性,描述了最近能够在单分子水平上实时追踪活细胞中效应蛋白的方法,并突出了该领域有待通过应用新方法解决的开放性问题。