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Searching for the two-photon brightest red fluorescent protein and its optimum excitation wavelength

机译:寻找两光子最亮的红色荧光蛋白及其最佳激发波长

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We study 2PA spectra of red fluorescent proteins (FPs), including DsRed2, mRFP, tagRFP, and mFruits in a wide range of excitation wavelengths, 600 - 1200 nm. For evaluation of mature FP extinction coefficient and concentration we propose a pure optical method which is based on Strickler - Berg equation, relating fluorescence radiative lifetime with molecular extinction coefficient. 2PA spectra and maximum cross sections are very sensitive to either changes in the chromophore structure (mOrange vs mRFP) or mutations in chromophore surrounding (DsRed and mFruits). All red FPs show two pronounced 2PA transitions, the first peaking in the 1000 - 1100-nm region, and the second - near 700 - 760 nm. For each region we have found a mutant, which is 3 - 4 times two-photon brighter than the benchmark EGFP.
机译:我们研究了红色荧光蛋白(FPs)的2PA光谱,包括600-1200 nm的宽激发波长范围内的DsRed2,mRFP,tagRFP和mFruits。为了评估成熟的FP消光系数和浓度,我们提出了一种基于Strickler-Berg方程的纯光学方法,该方法将荧光辐射寿命与分子消光系数相关联。 2PA光谱和最大截面对发色团结构的变化(mOrange与mRFP)或发色团周围的突变(DsRed和mFruits)非常敏感。所有红色FP均显示出两个明显的2PA跃迁,第一个跃迁在1000-1100 nm区域达到峰值,第二个跃迁在700-760 nm附近。对于每个区域,我们都发现了一个突变体,该突变体的亮度是基准EGFP的2光子亮度的3-4倍。

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