Rizzo Megan A, Piston David W
Biophys J. 2005 Feb;88(2):L14-6. doi: 10.1529/biophysj.104.055442. Epub 2004 Dec 21.
Detection of Forster resonance energy transfer (FRET) between fluorescent protein labeled targets is a valuable strategy for measurement of protein-protein interactions and other intracellular processes. Despite the utility of FRET, widespread application of this technique to biological problems and high-throughput screening has been limited by low-contrast measurement strategies that rely on the detection of sensitized emission or photodestruction of the sample. Here we report a FRET detection strategy based on detecting depolarized sensitized emission. In the absence of FRET, we show that fluorescence emission from a donor fluorescent protein is highly polarized. Depolarization of fluorescence emission is observed only in the presence of energy transfer. A simple detection strategy was adapted for fluorescence microscopy using both laser scanning and wide-field approaches. This approach is able to distinguish FRET between linked and unlinked Cerulean and Venus fluorescent proteins in living cells with a larger dynamic range than other approaches.
检测荧光蛋白标记靶标之间的福斯特共振能量转移(FRET)是测量蛋白质-蛋白质相互作用及其他细胞内过程的一种有价值的策略。尽管FRET具有实用性,但该技术在生物问题及高通量筛选中的广泛应用一直受到低对比度测量策略的限制,这些策略依赖于敏化发射检测或样品的光破坏。在此,我们报告一种基于检测去极化敏化发射的FRET检测策略。在不存在FRET的情况下,我们发现供体荧光蛋白的荧光发射高度极化。仅在存在能量转移时才观察到荧光发射的去极化。一种简单的检测策略适用于使用激光扫描和宽场方法的荧光显微镜。与其他方法相比,该方法能够在更大的动态范围内区分活细胞中连接和未连接的天蓝色和维纳斯荧光蛋白之间的FRET。