Mank Marco, Reiff Dierk F, Heim Nicola, Friedrich Michael W, Borst Alexander, Griesbeck Oliver
AG Zelluläre Dynamik, Abteilung Neuronale Informationsverarbeitung, Max-Planck-Institut für Neurobiologie 82152 Martinsried, Germany.
Biophys J. 2006 Mar 1;90(5):1790-6. doi: 10.1529/biophysj.105.073536. Epub 2005 Dec 9.
Genetically encoded calcium biosensors have become valuable tools in cell biology and neuroscience, but some aspects such as signal strength and response kinetics still need improvement. Here we report the generation of a FRET-based calcium biosensor employing troponin C as calcium-binding moiety that is fast, is stable in imaging experiments, and shows a significantly enhanced fluorescence change. These improvements were achieved by engineering magnesium and calcium-binding properties within the C-terminal lobe of troponin C and by the incorporation of circularly permuted variants of the green fluorescent protein. This sensor named TN-XL shows a maximum fractional fluorescence change of 400% in its emission ratio and linear response properties over an expanded calcium regime. When imaged in vivo at presynaptic motoneuron terminals of transgenic fruit flies, TN-XL exhibits highly reproducible fluorescence signals with the fastest rise and decay times of all calcium biosensors known so far.
基因编码钙生物传感器已成为细胞生物学和神经科学中有价值的工具,但在信号强度和反应动力学等方面仍有待改进。在此,我们报告了一种基于荧光共振能量转移(FRET)的钙生物传感器的产生,该传感器采用肌钙蛋白C作为钙结合部分,具有快速、在成像实验中稳定以及荧光变化显著增强的特点。这些改进是通过对肌钙蛋白C C末端叶内的镁和钙结合特性进行工程改造以及引入绿色荧光蛋白的环状排列变体实现的。这种名为TN-XL的传感器在其发射比率中显示出400%的最大荧光分数变化,并在扩展的钙范围内具有线性响应特性。当在转基因果蝇的突触前运动神经元末端进行体内成像时,TN-XL表现出高度可重复的荧光信号,其上升和衰减时间是迄今为止所有已知钙生物传感器中最快的。