Watching proteins in the wild: Fluorescence methods to study protein dynamics in living cells

被引:42
作者
Chamberlain, C [1 ]
Hahn, KM [1 ]
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
关键词
biosensor; dye; energy transfer; fluorescence; FRET; GFP; imaging; live cell; microscopy;
D O I
10.1034/j.1600-0854.2000.011002.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The advent of GFP imaging has led to a revolution in the study of live cell protein dynamics. Ease of access to fluorescently tagged proteins has led to their widespread application and demonstrated the power of studying protein dynamics in living cells. This has spurred development of next generation approaches enabling not only the visualization of protein movements, but correlation of a protein's dynamics with its changing structural state or ligand binding. Such methods make use of fluorescence resonance energy transfer and dyes that report changes in their environment, and take advantage of new chemistries for site-specific protein labeling.
引用
收藏
页码:755 / 762
页数:8
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