Goudsmits Joris M H, van Oijen Antoine M, Slotboom Dirk J
University of Groningen, Groningen, The Netherlands.
University of Groningen, Groningen, The Netherlands.
Methods Enzymol. 2017;594:101-121. doi: 10.1016/bs.mie.2017.05.009. Epub 2017 Jul 18.
Cells are delineated by a lipid bilayer that physically separates the inside from the outer environment. Most polar, charged, or large molecules require proteins to reduce the energetic barrier for passage across the membrane and to achieve transport rates that are relevant for life. Here, we describe techniques to visualize the functioning of membrane transport proteins with fluorescent probes at the single-molecule level. First, we explain how to produce membrane-reconstituted transporters with fluorescent labels. Next, we detail the construction of a microfluidic flow cell to image immobilized proteoliposomes on a total internal reflection fluorescence microscope. We conclude by describing the methods that are needed to analyze fluorescence movies and obtain useful single-molecule data.
细胞由脂质双层界定,脂质双层将细胞内部与外部环境物理分隔开来。大多数极性、带电或大分子需要蛋白质来降低跨膜转运的能量屏障,并实现与生命相关的转运速率。在这里,我们描述了在单分子水平上用荧光探针可视化膜转运蛋白功能的技术。首先,我们解释如何制备带有荧光标记的膜重组转运蛋白。接下来,我们详细介绍微流控流动池的构建,以便在全内反射荧光显微镜下对固定化蛋白脂质体进行成像。我们通过描述分析荧光电影和获得有用单分子数据所需的方法来结束本文。