Haraguchi Tokuko, Shimi Takeshi, Koujin Takako, Hashiguchi Noriyo, Hiraoka Yasushi
CREST Research Project, Kansai Advanced Research Center, Communications Research Laboratory, 588-2 Iwaoka, Iwaoka-cho, Nishi-ku, Kobe 651-2492, Japan.
Genes Cells. 2002 Sep;7(9):881-7. doi: 10.1046/j.1365-2443.2002.00575.x.
The spectral resolution of fluorescence microscope images in living cells is achieved by using a confocal laser scanning microscope equipped with grating optics. This capability of temporal and spectral resolution is especially useful for detecting spectral changes of a fluorescent dye; for example, those associated with fluorescence resonance energy transfer (FRET). Using the spectral imaging fluorescence microscope system, it is also possible to resolve emitted signals from fluorescent dyes that have spectra largely overlapping with each other, such as fluorescein isothiocyanate (FITC) and green fluorescent protein (GFP).
通过使用配备光栅光学元件的共聚焦激光扫描显微镜,可实现活细胞中荧光显微镜图像的光谱分辨率。这种时间和光谱分辨率的能力对于检测荧光染料的光谱变化特别有用;例如,那些与荧光共振能量转移(FRET)相关的变化。使用光谱成像荧光显微镜系统,还可以分辨来自光谱大部分相互重叠的荧光染料发出的信号,如异硫氰酸荧光素(FITC)和绿色荧光蛋白(GFP)。