Bielefeld University, Department of Chemistry, Biophysical Chemistry, 33615, Bielefeld, Germany.
Photochem Photobiol Sci. 2009 Nov;8(11):1517-28. doi: 10.1039/b9pp00050j. Epub 2009 Oct 6.
The introduction of time-resolved Fourier transform infrared (FT-IR) spectroscopy to biochemistry opened the possibility of monitoring the catalytic mechanism of proteins along their reaction pathways. The infrared approach is very fruitful, particularly in the application to membrane proteins where NMR and X-ray crystallography are challenged by the size and protein hydrophobicity, as well as by their limited time-resolution. Here, we summarize the principles and experimental realizations of time-resolved FT-IR spectroscopy developed in our group and compare with aspects emerging from other laboratories. Examples of applications to retinal proteins and energy transduction complexes are reviewed, which emphasize the impact of time-resolved FT-IR spectroscopy on the understanding of protein reactions on the level of single bonds.
时间分辨傅里叶变换红外(FT-IR)光谱学在生物化学中的引入开辟了沿反应途径监测蛋白质催化机制的可能性。红外方法非常有成效,特别是在膜蛋白的应用中,NMR 和 X 射线晶体学受到蛋白质大小和疏水性以及有限的时间分辨率的挑战。在这里,我们总结了我们小组开发的时间分辨 FT-IR 光谱学的原理和实验实现,并与其他实验室出现的方面进行了比较。回顾了应用于视网膜蛋白和能量传递复合物的实例,这些实例强调了时间分辨 FT-IR 光谱学对理解单键水平上蛋白质反应的影响。