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一种用于分析蛋白质荧光动力学的亚纳秒分辨荧光分光光度计。

A subnanosecond resolving spectrofluorimeter for the analysis of protein fluorescence kinetics.

作者信息

van Hoek A, Vervoort J, Visser A J

出版信息

J Biochem Biophys Methods. 1983 May;7(3):243-54. doi: 10.1016/0165-022x(83)90033-7.

Abstract

A spectrofluorometer is described consisting of an excitation source, optics, detector and time resolving electronics. The excitation source consists of a mode-locked Ar ion laser, which synchronously pumps a dye laser, followed by a frequency doubling device. The repetition frequency of the U.V. pulses (FWHM some ps) has been reduced by an extra-cavity electro-optical modulator. Provisions have been made in the optical configuration to determine both time-resolved fluorescence spectra and fluorescence anisotropy decay curves. The commercially available electronics have been optimized for maximum time resolution. The spectral output of the excitation source is confined between 280 and 310 nm, which encompasses the region for eliciting protein fluorescence. The performance of the complete system has been tested with single lifetime standards like p-terphenyl in cyclohexane or with N-acetyl-L-tryptophanamide in pH 7.5 buffer. Serum albumins from human and bovine sources have been employed as examples for time resolved fluorescence spectra and for the demonstration of anisotropy decay curves. Using these methods protein dynamics in the (sub)nanosecond time region can be directly explored.

摘要

本文描述了一种荧光分光光度计,它由激发源、光学器件、探测器和时间分辨电子设备组成。激发源由一个锁模氩离子激光器组成,该激光器同步泵浦一个染料激光器,随后是一个倍频装置。紫外脉冲(半高宽约为皮秒)的重复频率通过一个外腔电光调制器降低。在光学配置中已作了安排,以测定时间分辨荧光光谱和荧光各向异性衰减曲线。市售的电子设备已针对最大时间分辨率进行了优化。激发源的光谱输出限制在280至310纳米之间,该区域涵盖了激发蛋白质荧光的区域。整个系统的性能已用环己烷中的对三联苯或pH 7.5缓冲液中的N-乙酰-L-色氨酸酰胺等单寿命标准进行了测试。人源和牛源血清白蛋白已被用作时间分辨荧光光谱的示例以及各向异性衰减曲线的演示。使用这些方法可以直接探索(亚)纳秒时间区域内的蛋白质动力学。

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