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高速光学切片荧光寿命成像技术可用于研究活细胞信号传导事件。

High speed optically sectioned fluorescence lifetime imaging permits study of live cell signaling events.

作者信息

Grant David M, McGinty J, McGhee E J, Bunney T D, Owen D M, Talbot C B, Zhang W, Kumar S, Munro I, Lanigan P M, Kennedy G T, Dunsby C, Magee A I, Courtney P, Katan M, Neil M A A, French P M W

出版信息

Opt Express. 2007 Nov 26;15(24):15656-73. doi: 10.1364/oe.15.015656.

Abstract

We present a time domain optically sectioned fluorescence lifetime imaging (FLIM) microscope developed for high-speed live cell imaging. This single photon excited system combines wide field parallel pixel detection with confocal sectioning utilizing spinning Nipkow disc microscopy. It can acquire fluorescence lifetime images of live cells at up to 10 frames per second (fps), permitting high-speed FLIM of cell dynamics and protein interactions with potential for high throughput cell imaging and screening applications. We demonstrate the application of this FLIM microscope to real-time monitoring of changes in lipid order in cell membranes following cholesterol depletion using cyclodextrin and to the activation of the small GTP-ase Ras in live cells using FRET.

摘要

我们展示了一种为高速活细胞成像而开发的时域光学切片荧光寿命成像(FLIM)显微镜。这个单光子激发系统将宽场并行像素检测与利用旋转尼普科夫盘显微镜的共聚焦切片相结合。它能够以每秒高达10帧(fps)的速度获取活细胞的荧光寿命图像,从而实现对细胞动态和蛋白质相互作用的高速FLIM成像,具有用于高通量细胞成像和筛选应用的潜力。我们展示了这种FLIM显微镜在使用环糊精耗尽胆固醇后实时监测细胞膜中脂质有序性变化以及使用荧光共振能量转移(FRET)在活细胞中监测小GTP酶Ras激活方面的应用。

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