Dark dyes-bright complexes: fluorogenic protein labeling

被引:53
作者
Bruchez, Marcel P. [1 ,2 ,3 ]
机构
[1] Carnegie Mellon Univ, Mol Biosensor & Imaging Ctr, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
[3] Carnegie Mellon Univ, Dept Biol Sci, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
STRUCTURED-ILLUMINATION MICROSCOPY; THROUGHPUT FLOW-CYTOMETRY; LIVE-CELL; ACTIVATING PROTEINS; NO-WASH; LOCALIZATION MICROSCOPY; SURFACE-PROTEINS; CYANINE DYES; PROBES; FLUORESCENCE;
D O I
10.1016/j.cbpa.2015.05.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Complexes formed between organic dyes and genetically encoded proteins combine the advantages of stable and tunable fluorescent molecules and targetable, biologically integrated labels. To overcome the challenges imposed by labeling with bright fluorescent dyes, a number of approaches now exploit chemical or environmental changes to control the properties of a bound dye, converting dyes from a weakly fluorescent state to a bright, easily detectable complex. Optimized, such approaches avoid the need for removal of unbound dyes, facilitate rapid and simple assays in cultured cells and enable hybrid labeling to function more robustly in living model organisms.
引用
收藏
页码:18 / 23
页数:6
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