A genetically encoded fluorescent sensor of ERK activity

被引:261
作者
Harvey, Christopher D. [1 ,2 ]
Ehrhardt, Anka G. [3 ,4 ]
Cellurale, Cristina [3 ,4 ]
Zhong, Haining [1 ]
Yasuda, Ryohei [5 ]
Davis, Roger J. [3 ,4 ]
Svoboda, Karel [1 ,2 ]
机构
[1] Howard Hughes Med Inst, Ashburn, VA 20147 USA
[2] Cold Spring Harbor Lab, Watson Sch Biol Sci, Cold Spring Harbor, NY 11724 USA
[3] Univ Massachusetts, Sch Med, Howard Hughes Med Inst, Worcester, MA 01605 USA
[4] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[5] Duke Univ, Dept Neurobiol, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
fluorescence lifetime imaging microscopy; FRET; MAPK;
D O I
10.1073/pnas.0804598105
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
The activity of the ERK has complex spatial and temporal dynamics that are important for the specificity of downstream effects. However, current biochemical techniques do not allow for the measurement of ERK signaling with fine spatiotemporal resolution. We developed a genetically encoded, FRET-based sensor of ERK activity (the extracellular signal-regulated kinase activity reporter, EKAR), optimized for signal-to-noise ratio and fluorescence lifetime imaging. EKAR selectively and reversibly reported ERK activation in HEK293 cells after epidermal growth factor stimulation. EKAR signals were correlated with ERK phosphorylation, required ERK activity, and did not report the activities of JNK or p38. EKAR reported ERK activation in the dendrites and nucleus of hippocampal pyramidal neurons in brain slices after theta-burst stimuli or trains of back-propagating action potentials. EKAR therefore permits the measurement of spatiotemporal ERK signaling dynamics in living cells, including in neuronal compartments in intact tissues.
引用
收藏
页码:19264 / 19269
页数:6
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