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Synthesis and characterization of a combined fluorescence phosphorescence and electron paramagnetic resonance probe

机译:组合荧光磷光和电子顺磁共振探针的合成与表征

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A spin-labeled derivative of eosin was chemically synthesized from 5-aminoeosin and the nitroxide spin label 2,2,5,5- tetramethylpyrrolin-1-oxyl-3-carboxylic acid. Following determination of the chemical identity of the spin-labeled eosin (5-SLE) by FAB mass spectroscopy, its optical and magnetic resonance spectroscopic properties were characterized in aqueous solution and compared to a diamagnetic eosin derivative, 5- acetamido eosin (5-AcE). The visible light absorption maximum of 5-SLE was 518 nm, the same as for 5-AcE. The fluorescence quantum yield of 5-SLE was only reduced by approximately 10% relative to 5-AcE, and the fluorescence lifetime was marginally reduced relative to 5-AcE. The phosphorescence lifetime and yield for 5-SLE were very similar to those for 5-AcE. The phosphorescence yield of 5-SLE bound noncovalently to BSA was reduced by approximately 60% relative to 5-AcE, and the phosphorescence lifetime reduced from approximately 2.4 msec (5-AcE) to 1.6 msec (5-SLE). Reduction of the nitroxide moiety of the 5-SLE with sodium ascorbate resulted in minimal changes in the fluorescence and phosphorescence quantum yields and lifetimes. This indicated that the unpaired electron of the nitroxide spin label did not seriously affect the optical spectroscopic characteristics of the spin-labeled eosin molecule. The quantum yields and lifetimes of 5-SLE were still quite acceptable for time-resolved fluorescence and phosphorescence studies. The electron paramagnetic resonance (EPR) spectrum of 5-SLE in aqueous solution has a lineshape consistent with a molecule the size of 5-SLE undergoing rapid rotational reorientation. When bound to BSA, the EPR spectrum of 5-SLE was broadened to a near slow motion limit for EPR, as expected for the relatively slowly rotating protein-5-SLE complex. Time-resolved phosphorescence anisotropy and saturation transfer EPR (ST-EPR) experiments with samples of 5-SLE bound to BSA in solutions of varying glycerol concentrations at 2$DGR@C demonstrated that this combined probe is suitable for monitoring rotational dynamics of macromolecular systems over the appropriate time ranges. These studies have shown that one combined optical and EPR probe, 5-SLE, can be employed in the full range of fluorescence, phosphorescence, EPR, and ST-EPR spectroscopies.
机译:从5- aminoooosin和氮氧化物旋旋标记2,2,5,5-四甲基吡咯蛋白-1-氧基-3-羧酸的旋转标记的曙红衍生物化学合成。通过Fab质谱法测定旋转标记的曙红(5-SES)的化学特性,其光学和磁共振光谱性能在水溶液中表征,与二碳酸二辛衍生物,5-乙酰氨基胺(5-Ace)相比)。可见光吸收最大5-SL为518nm,与5°相同。相对于5-ACE的荧光量子产率仅减少约10%,相对于5-ACE的荧光寿命略微降低。磷光寿命和5SE的产率与5-Ace的磷光寿命和产率非常相似。相对于5-ACE的5-SLE非共价荧光率为约60%的磷光率降低,磷光寿命从大约2.4毫秒(5-ACE)降低至1.6毫秒(5SE)。用抗坏血酸钠的5-SL的硝基氧化物部分的氧化物部分导致荧光和磷光量子产率和寿命的最小变化。这表明硝基X旋转标签的未配对的电子没有严重影响旋转标记的eosin分子的光学光谱特性。对于时间解决的荧光和磷光研究,量子产率和5S的寿命仍然是非常可接受的。在水溶液中为5-SLE的电子顺磁共振(EPR)光谱具有与分子达到快速旋转重新定向的分子括号一致的线。当与BSA绑定时,通常对EPR的EPR光谱扩大到EPR的近慢动作限制,如相对缓慢的旋转蛋白-5 -LEL复合物的预期。时间分离的磷光各向异性和饱和度转移EPR(ST-EPR)在2 $ DGR @ C的不同甘油浓度的溶液中与BSA的样品进行了实验,在2 $ DGR @ C的溶液中证明了该组合探针适用于监测大分子系统的旋转动力学在适当的时间范围内。这些研究表明,一种组合的光学和EPR探针,5SL,可以在全范围的荧光,磷光,EPR和ST-EPR光谱中使用。

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