European Molecular Biology Laboratory, Advanced Light Microscopy Facility, Meyerhofstr 1, 69117 Heidelberg, Germany.
J Biomed Opt. 2012 Jan;17(1):011010. doi: 10.1117/1.JBO.17.1.011010.
Fluorescence resonance energy transfer (FRET) efficiency measurements based on acceptor photobleaching of yellow fluorescent protein (YFP) are affected by the fact that bleaching of YFP produces a fluorescent species that is detectable in cyan fluorescent protein (CFP) image channels. The presented quantitative measurement of this conversion makes it possible to correct the obtained FRET signal to increase the accuracy of intensity based CFP/YFP FRET measurements. The described method can additionally be used to compare samples with very different fluorescence levels.
基于黄色荧光蛋白(YFP)的光漂白的荧光共振能量转移(FRET)效率测量受到这样一个事实的影响,即 YFP 的漂白会产生一种在青色荧光蛋白(CFP)图像通道中可检测到的荧光物质。该方法对这种转化进行了定量测量,从而可以校正所获得的 FRET 信号,以提高基于强度的 CFP/YFP FRET 测量的准确性。该方法还可用于比较荧光水平差异非常大的样品。