A genetically encoded Forster resonance energy transfer sensor for monitoring in vivo trehalose-6-phosphate dynamics

被引:21
|
作者
Peroza, Estevao A. [1 ]
Ewald, Jennifer C. [2 ]
Parakkal, Geetha [1 ]
Skotheim, Jan M. [2 ]
Zamboni, Nicola [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Mol Syst Biol, CH-8093 Zurich, Switzerland
[2] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
关键词
Trehalose-6-phosphate; FRET sensor; Glycolysis regulation; ESCHERICHIA-COLI; SACCHAROMYCES-CEREVISIAE; TREHALOSE; 6-PHOSPHATE; GENE; GLYCOLYSIS; FAMILY; EXPRESSION; REGULATOR; TRANSPORT; SYNTHASE;
D O I
10.1016/j.ab.2014.12.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Trehalose-6-phosphate is a pivotal regulator of sugar metabolism, growth, and osmotic equilibrium in bacteria, yeasts, and plants. To directly visualize the intracellular levels of intracellular trehalose-6-phosphate, we developed a series of specific Forster resonance energy transfer (FRET) sensors for in vivo microscopy. We demonstrated real-time monitoring of regulation in the trehalose pathway of Escherichia con. In Saccharomyces cerevisiae, we could show that the concentration of free trehalose-6-phosphate during growth on glucose is in a range sufficient for inhibition of hexokinase. These findings support the hypothesis of trehalose-6-phosphate as the effector of a negative feedback system, similar to the inhibition of hexokinase by glucose-6-phosphate in mammalian cells and controlling glycolytic flux. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
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