Chai Liuying, Zhang Jianwei, Zhang Lili, Chen Tongsheng
J Biomed Opt. 2015 Mar;20(3):037008. doi: 10.1117/1.JBO.20.3.037008.
Spectral measurement of fluorescence resonance energy transfer (FRET), spFRET, is a widely used FRET quantification method in living cells today. We set up a spectrometer-microscope platform that consists of a miniature fiber optic spectrometer and a widefield fluorescence microscope for the spectral measurement of absolute FRET efficiency (E) and acceptor-to-donor concentration ratio (R(C)) in single living cells. The microscope was used for guiding cells and the spectra were simultaneously detected by the miniature fiber optic spectrometer. Moreover, our platform has independent excitation and emission controllers, so different excitations can share the same emission channel. In addition, we developed a modified spectral FRET quantification method (mlux-FRET) for the multiple donors and multiple acceptors FRET construct (mD∼nA) sample, and we also developed a spectra-based 2-channel acceptor-sensitized FRET quantification method (spE-FRET). We implemented these modified FRET quantification methods on our platform to measure the absolute E and R(C) values of tandem constructs with different acceptor/donor stoichiometries in single living Huh-7 cells.
荧光共振能量转移(FRET)的光谱测量,即单光子荧光共振能量转移(spFRET),是当今活细胞中广泛使用的FRET定量方法。我们搭建了一个光谱仪 - 显微镜平台,该平台由一台微型光纤光谱仪和一台宽场荧光显微镜组成,用于测量单个活细胞中绝对FRET效率(E)和受体与供体浓度比(R(C))的光谱。显微镜用于引导细胞,光谱由微型光纤光谱仪同时检测。此外,我们的平台具有独立的激发和发射控制器,因此不同的激发可以共享同一个发射通道。另外,我们针对多供体和多受体FRET构建体(mD∼nA)样品开发了一种改进的光谱FRET定量方法(mlux - FRET),还开发了一种基于光谱的双通道受体敏化FRET定量方法(spE - FRET)。我们在我们的平台上实施了这些改进的FRET定量方法,以测量单个活Huh - 7细胞中具有不同受体/供体化学计量比的串联构建体的绝对E和R(C)值。