首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Spectroscopic Studies of Model Photo-Receptors: Validation of a Nanosecond Time-Resolved Micro-Spectrophotometer Design Using Photoactive Yellow Protein and α-Phycoerythrocyanin
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Spectroscopic Studies of Model Photo-Receptors: Validation of a Nanosecond Time-Resolved Micro-Spectrophotometer Design Using Photoactive Yellow Protein and α-Phycoerythrocyanin

机译:模型感光体的光谱学研究:使用光敏黄色蛋白和α-藻红蛋白的纳秒级时间分辨微分光光度计设计的验证

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摘要

Time-resolved spectroscopic experiments have been performed with protein in solution and in crystalline form using a newly designed microspectrophotometer. The time-resolution of these experiments can be as good as two nanoseconds (ns), which is the minimal response time of the image intensifier used. With the current setup, the effective time-resolution is about seven ns, determined mainly by the pulse duration of the nanosecond laser. The amount of protein required is small, on the order of 100 nanograms. Bleaching, which is an undesirable effect common to photoreceptor proteins, is minimized by using a millisecond shutter to avoid extensive exposure to the probing light. We investigate two model photoreceptors, photoactive yellow protein (PYP), and α-phycoerythrocyanin (α-PEC), on different time scales and at different temperatures. Relaxation times obtained from kinetic time-series of difference absorption spectra collected from PYP are consistent with previous results. The comparison with these results validates the capability of this spectrophotometer to deliver high quality time-resolved absorption spectra.
机译:使用新设计的显微分光光度计,已经对溶液中的蛋白质和晶体形式的蛋白质进行了时间分辨光谱实验。这些实验的时间分辨率可以高达2纳秒(ns),这是所用图像增强器的最短响应时间。在当前设置下,有效时间分辨率约为7 ns,主要由纳秒激光器的脉冲持续时间决定。所需的蛋白质量很小,大约为100纳克。漂白是感光蛋白常见的不良影响,可通过使用毫秒快门来避免暴露于探测光下,从而最大程度地减少漂白。我们在不同的时间尺度和不同的温度下研究了两种模型感光器,即光敏性黄色蛋白(PYP)和α-藻红蛋白(α-PEC)。从PYP收集的差异吸收光谱的动力学时间序列获得的弛豫时间与先前的结果一致。与这些结果的比较验证了该分光光度计提供高质量的时间分辨吸收光谱的能力。

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