Dependence of fluorescent protein brightness on protein concentration in solution and enhancement of it

被引:40
|
作者
Morikawa, Takamitsu J. [1 ]
Fujita, Hideaki [2 ,4 ]
Kitamura, Akira [5 ]
Horio, Takashi [5 ]
Yamamoto, Johtaro [5 ]
Kinjo, Masataka [5 ]
Sasaki, Akira [6 ]
Machiyama, Hiroaki [2 ,4 ]
Yoshizawa, Keiko [4 ]
Ichimura, Taro [4 ]
Imada, Katsumi [7 ]
Nagai, Takeharu [1 ,3 ,4 ]
Watanabe, Tomonobu M. [4 ,8 ]
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, 1-3 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Osaka Univ, WPI, Immunol Frontier Res Ctr, 1-3 Yamadaoka, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Inst Sci & Ind Res, Ibaraki, Osaka 5650873, Japan
[4] RIKEN, Quantitat Biol Ctr QBiC, Suita, Osaka 5650874, Japan
[5] Hokkaido Univ, Fac Adv Life Sci, Sapporo, Hokkaido 0010021, Japan
[6] Natl Inst Adv Ind Sci & Technol, Biomed Res Inst, Tsukuba, Ibaraki 3058566, Japan
[7] Osaka Univ, Grad Sch Sci, Dept Macromol Sci, Toyonaka, Osaka 5650043, Japan
[8] Japan Sci & Technol Agcy, PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 3320012, Japan
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
日本科学技术振兴机构;
关键词
IMAGE CORRELATION SPECTROSCOPY; OSMOTIC-PRESSURE; DYNAMICS; VISCOSITY; CELLS; DIFFUSION; INCREASE; SHIFTS; TOOL; RED;
D O I
10.1038/srep22342
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fluorescent proteins have been widely used in biology because of their compatibility and varied applications in living specimens. Fluorescent proteins are often undesirably sensitive to intracellular conditions such as pH and ion concentration, generating considerable issues at times. However, harnessing these intrinsic sensitivities can help develop functional probes. In this study, we found that the fluorescence of yellow fluorescent protein (YFP) depends on the protein concentration in the solution and that this dependence can be enhanced by adding a glycine residue in to the YFP; we applied this finding to construct an intracellular protein-crowding sensor. A Frster resonance energy transfer (FRET) pair, involving a cyan fluorescent protein (CFP) insensitive to protein concentration and a glycine-inserted YFP, works as a genetically encoded probe to evaluate intracellular crowding. By measuring the fluorescence of the present FRET probe, we were able to detect dynamic changes in protein crowding in living cells.
引用
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页数:13
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