Toh Wei Hong, Houghton Fiona J, Chia Pei Zhi Cheryl, Ramdzan Yasmin M, Hatters Danny M, Gleeson Paul A
Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, VIC, 3010, Australia.
Methods Mol Biol. 2015;1270:227-38. doi: 10.1007/978-1-4939-2309-0_17.
Pulse shape analysis (PulSA) is a flow cytometry-based method that involves the measurement of the pulse width and height of a fluorescently labeled molecule simultaneously, enabling a multidimensional analysis of protein localization in a cell at high speed and throughput. We have used the method to detect morphological changes in organelles such as Golgi fragmentation, track protein trafficking from the cell surface, and also discriminate cells with different target protein localizations such as the Golgi, lyso-endosomal network, and the plasma membrane. Here, we describe the basic experimental setup and analytical methods for performing PulSA to examine membrane trafficking processes. We illustrate in particular the application of PulSA for monitoring the trafficking of the membrane-bound enzyme furin and morphological changes to the Golgi caused by Brefeldin A.
脉冲形状分析(PulSA)是一种基于流式细胞术的方法,该方法涉及同时测量荧光标记分子的脉冲宽度和高度,从而能够对细胞内蛋白质定位进行高速、高通量的多维分析。我们已使用该方法检测细胞器的形态变化,如高尔基体碎片化,追踪蛋白质从细胞表面的运输,还能区分具有不同靶蛋白定位的细胞,如高尔基体、溶酶体 - 内体网络和质膜。在此,我们描述了进行PulSA以检查膜运输过程的基本实验设置和分析方法。我们特别举例说明了PulSA在监测膜结合酶弗林蛋白酶的运输以及布雷菲德菌素A引起的高尔基体形态变化方面的应用。