Hawley Teresa S, Herbert Donald J, Eaker Shannon S, Hawley Robert G
Flow Cytometry Facility and Hematopoiesis Department, Holland Laboratory, American Red Cross, Rockville, MD, USA.
Methods Mol Biol. 2004;263:219-38. doi: 10.1385/1-59259-773-4:219.
Reporters based on the green fluorescent protein (GFP) from the jellyfish Aequorea victoria and GFP-like proteins from other marine organisms provide valuable tools to monitor gene transfer and expression noninvasively in living cells. Stable cell lines were generated from the Sp2/0-Ag14 hybridoma that express up to three spectral enhanced versions of GFP, the enhanced cyan fluorescent protein (ECFP), the enhanced green fluorescent protein (EGFP), and the enhanced yellow fluorescent protein (EYFP), and/or a variant of the Discosoma coral red fluorescent protein (DsRed). The panel of lines was used to demonstrate a flow cytometric procedure for simultaneous analysis of all four fluorescent proteins that utilizes dual-laser excitation at 488 nm and 407 nm. Additional schemes for simultaneous detection of two, three or four of these fluorescent proteins are also presented.
基于来自维多利亚多管水母的绿色荧光蛋白(GFP)以及其他海洋生物的类GFP蛋白的报告基因,为在活细胞中无创监测基因转移和表达提供了有价值的工具。从Sp2/0-Ag14杂交瘤细胞系中构建出稳定细胞系,这些细胞系可表达多达三种光谱增强型GFP,即增强型青色荧光蛋白(ECFP)、增强型绿色荧光蛋白(EGFP)和增强型黄色荧光蛋白(EYFP),以及/或者盘状珊瑚红色荧光蛋白(DsRed)的一种变体。该细胞系面板用于展示一种流式细胞术程序,该程序利用488nm和407nm的双激光激发同时分析所有四种荧光蛋白。文中还介绍了同时检测其中两种、三种或四种荧光蛋白的其他方案。