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Using Fractional Intensities of Time-resolved Fluorescence to Sensitively Quantify NADH/NAD+ with Genetically Encoded Fluorescent Biosensors

机译:使用时间分辨荧光的分数强度通过遗传编码的荧光生物传感器灵敏地定量NADH / NAD +

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摘要

In this paper, we propose a novel and sensitive ratiometric analysis method that uses the fractional intensities of time-resolved fluorescence of genetically encoded fluorescent NADH/NAD+ biosensors, Peredox, SoNar, and Frex. When the conformations of the biosensors change upon NADH/NAD+ binding, the fractional intensities (α i τ i) have opposite changing trends. Their ratios could be exploited to quantify NADH/NAD+ levels with a larger dynamic range and higher resolution versus commonly used fluorescence intensity and lifetime methods. Moreover, only one excitation and one emission wavelength are required for this ratiometric measurement. This eliminates problems of traditional excitation-ratiometric and emission-ratiometric methods. This method could be used to simplify the design and achieve highly sensitive analyte quantification of genetically encoded fluorescent biosensors. Wide potential applications could be developed for imaging live cell metabolism based on this new method.
机译:在本文中,我们提出了一种新颖而灵敏的比例分析方法,该方法使用了遗传编码的荧光NADH / NAD + 生物传感器,Peredox,SoNar和Frex的时间分辨荧光的分数强度。当生物传感器的构型随NADH / NAD + 结合而改变时,分数强度(αiτi)具有相反的变化趋势。与常用的荧光强度和寿命方法相比,可以利用它们的比率来定量NADH / NAD + 水平,具有更大的动态范围和更高的分辨率。此外,该比例测量仅需要一个激发和一个发射波长。这就消除了传统的激励-比率和发射-比率方法的问题。此方法可用于简化设计并实现遗传编码的荧光生物传感器的高灵敏度分析物定量。基于这种新方法,可以开发用于活细胞代谢成像的广泛潜在应用。

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