Supportive Center for Brain Research, National Institute for Physiological Sciences, Okazaki, Aichi, 444-8585, Japan.
Department of Physiological Sciences, Sokendai (The Graduate University for Advanced Studies), Okazaki, Aichi, 444-8585, Japan.
Sci Rep. 2017 Jul 28;7(1):6791. doi: 10.1038/s41598-017-07002-4.
Fluorescence lifetime imaging microscopy (FLIM)-based Förster resonance energy transfer (FRET) measurement (FLIM-FRET) is one of the powerful methods for imaging of intracellular protein activities such as protein-protein interactions and conformational changes. Here, using saturation mutagenesis, we developed a dark yellow fluorescent protein named ShadowY that can serve as an acceptor for FLIM-FRET. ShadowY is spectrally similar to the previously reported dark YFP but has a much smaller quantum yield, greater extinction coefficient, and superior folding property. When ShadowY was paired with mEGFP or a Clover mutant (Clover) and applied to a single-molecule FRET sensor to monitor a light-dependent conformational change of the light-oxygen-voltage domain 2 (LOV2) in HeLa cells, we observed a large FRET signal change with low cell-to-cell variability, allowing for precise measurement of individual cell responses. In addition, an application of ShadowY to a separate-type Ras FRET sensor revealed an EGF-dependent large FRET signal increase. Thus, ShadowY in combination with mEGFP or Clover is a promising FLIM-FRET acceptor.
基于荧光寿命成像显微镜(FLIM)的Förster 共振能量转移(FRET)测量(FLIM-FRET)是一种强大的方法,可用于成像细胞内蛋白质活性,如蛋白质-蛋白质相互作用和构象变化。在这里,我们通过饱和突变,开发了一种名为 ShadowY 的深黄色荧光蛋白,它可用作 FLIM-FRET 的受体。ShadowY 在光谱上与之前报道的深黄色 YFP 相似,但量子产率更小、消光系数更大、折叠性能更好。当 ShadowY 与 mEGFP 或 Clover 突变体(Clover)配对,并应用于单分子 FRET 传感器来监测 HeLa 细胞中光氧电压域 2(LOV2)的光依赖性构象变化时,我们观察到了大的 FRET 信号变化,细胞间变异性低,能够精确测量单个细胞的反应。此外,ShadowY 在另一种 Ras FRET 传感器中的应用显示出 EGF 依赖性的大 FRET 信号增加。因此,ShadowY 与 mEGFP 或 Clover 结合是一种很有前途的 FLIM-FRET 受体。