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A Genetically Encoded Fluorescent Sensor Of Erk Activity

机译:基因编码的Erk活动的荧光传感器。

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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.
机译:ERK的活动具有复杂的时空动态,对于下游效应的特异性很重要。但是,当前的生物化学技术不允许以良好的时空分辨率测量ERK信号。我们开发了一种基于基因编码的基于FRET的ERK活性传感器(细胞外信号调节激酶活性报告剂EKAR),针对信噪比和荧光寿命成像进行了优化。在表皮生长因子刺激后,EKAR选择性且可逆地报告了HEK293细胞中的ERK激活。 EKAR信号与ERK磷酸化,所需的ERK活性相关,并且未报告JNK或p38的活性。 EKAR报道了θ-爆发刺激或一系列反向传播的动作电位后,脑切片中海马锥体神经元的树突和核中的ERK激活。因此,EKAR可以测量活细胞(包括完整组织中神经元区室)中时空ERK信号的动态变化。

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