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光漂白绿色荧光蛋白可揭示活细胞内的蛋白质动态变化。

Photobleaching GFP reveals protein dynamics inside live cells.

作者信息

White J, Stelzer E

机构信息

Cell Biology and Cell Biophysics Programme, European Molecular Biology Laboratory, Heidelberg, Germany.

出版信息

Trends Cell Biol. 1999 Feb;9(2):61-5. doi: 10.1016/s0962-8924(98)01433-0.

DOI:10.1016/s0962-8924(98)01433-0
PMID:10087620
Abstract

Cell biologists have used photobleaching to investigate the lateral mobility of fluorophores on the cell surface since the 1970s. Fusions of green fluorescent protein (GFP) to specific proteins extend photobleaching techniques to the investigation of protein dynamics within the cell, leading to renewed interest in photobleaching experiments. This article revisits general photobleaching concepts, reviews what can be learned from them and discusses applications illustrating the potential of photobleaching GFP fusion proteins inside living cells.

摘要

自20世纪70年代以来,细胞生物学家一直使用光漂白技术来研究细胞表面荧光团的侧向流动性。绿色荧光蛋白(GFP)与特定蛋白质的融合将光漂白技术扩展到细胞内蛋白质动力学的研究,引发了人们对光漂白实验的新兴趣。本文回顾了一般的光漂白概念,总结了从中可以学到的知识,并讨论了相关应用,展示了在活细胞内对GFP融合蛋白进行光漂白的潜力。

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Photobleaching GFP reveals protein dynamics inside live cells.光漂白绿色荧光蛋白可揭示活细胞内的蛋白质动态变化。
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Sensitivity of CFP/YFP and GFP/mCherry pairs to donor photobleaching on FRET determination by fluorescence lifetime imaging microscopy in living cells.在活细胞中通过荧光寿命成像显微镜进行荧光共振能量转移测定时,CFP/YFP和GFP/mCherry对供体光漂白的敏感性。
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