Micalis Institute, INRA, AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, France.
Methods Mol Biol. 2020;2101:123-133. doi: 10.1007/978-1-0716-0219-5_8.
MreB proteins are actin homologs present in nonspherical bacteria. They assemble into membrane-associated discrete filamentous structures that exhibit different dynamic behaviors along the bacterial sidewalls. Total internal reflection fluorescence (TIRF) microscopy, a sensitive method for studying molecular events at cell surfaces with high contrast and temporal resolution, is a method of choice to characterize the localization and dynamics of cortical MreB assemblies in vivo. This chapter describes the methods for visualizing fluorescently tagged MreB proteins in live Bacillus subtilis cells. We detail how to (1) grow B. subtilis strains for reproducible TIRF observations, (2) immobilize cells on agarose pads and (3) in CellASIC microfluidic plates, and (4) acquire TIRF images and time lapses.
MreB 蛋白是存在于非球形细菌中的肌动蛋白同源物。它们组装成膜相关的离散丝状结构,沿细菌侧壁表现出不同的动态行为。全内反射荧光 (TIRF) 显微镜是一种高对比度和高时间分辨率的研究细胞表面分子事件的敏感方法,是用于体内表征皮质 MreB 组装体定位和动力学的首选方法。本章描述了在活枯草芽孢杆菌细胞中可视化荧光标记 MreB 蛋白的方法。我们详细介绍了如何 (1) 培养枯草芽孢杆菌菌株以进行可重复的 TIRF 观察,(2) 将细胞固定在琼脂糖垫和 (3) CellASIC 微流控板上,以及 (4) 获取 TIRF 图像和时间推移。