Max-Planck-Institut für Quantenoptik, Hans-Kopfermann-Straße 1, 85748 Garching, Germany.
Lehrstuhl für Experimental Physik, Ludwig-Maximilians-Universität München, Am Coulombwall 1, 85748 Garching, Germany.
Molecules. 2021 Nov 16;26(22):6893. doi: 10.3390/molecules26226893.
Proteins play an important role in biological and biochemical processes taking place in the living system. To uncover these fundamental processes of the living system, it is an absolutely necessary task to understand the structure and dynamics of the protein. Vibrational spectroscopy is an established tool to explore protein structure and dynamics. In particular, two-dimensional infrared (2DIR) spectroscopy has already proven its versatility to explore the protein structure and its ultrafast dynamics, and it has essentially unprecedented time resolutions to observe the vibrational dynamics of the protein. Providing several examples from our theoretical and experimental efforts, it is established here that two-dimensional vibrational spectroscopy provides exceptionally more information than one-dimensional vibrational spectroscopy. The structural information of the protein is encoded in the position, shape, and strength of the peak in 2DIR spectra. The time evolution of the 2DIR spectra allows for the visualisation of molecular motions.
蛋白质在生命系统中发生的生物和生化过程中起着重要作用。为了揭示生命系统的这些基本过程,了解蛋白质的结构和动力学是一项绝对必要的任务。振动光谱是探索蛋白质结构和动力学的一种成熟工具。特别是,二维红外(2DIR)光谱已经证明了其探索蛋白质结构及其超快动力学的多功能性,并且它具有观察蛋白质振动动力学的本质上前所未有的时间分辨率。通过提供我们的理论和实验努力的几个例子,这里已经确定二维振动光谱比一维振动光谱提供了更多的信息。蛋白质的结构信息编码在 2DIR 光谱中峰的位置、形状和强度。2DIR 光谱的时间演化允许对分子运动进行可视化。