Heugen U, Schwaab G, Bründermann E, Heyden M, Yu X, Leitner D M, Havenith M
Lehrstuhl für Physikalische Chemie II, Ruhr-Universität Bochum, 44780 Bochum, Germany.
Proc Natl Acad Sci U S A. 2006 Aug 15;103(33):12301-6. doi: 10.1073/pnas.0604897103. Epub 2006 Aug 8.
The dynamics of water surrounding a solute is of fundamental importance in chemistry and biology. The properties of water molecules near the surface of a bio-molecule have been the subject of numerous, sometimes controversial experimental and theoretical studies, with some suggesting the existence of rather rigid water structures around carbohydrates and proteins [Pal, S. K., Peon, J., Bagchi, B. and Zewail A. H. (2002) J. Phys. Chem. B 106, 12376-12395]. Hydrogen bond rearrangement in water occurs on the picosecond time scale, so relevant experiments must access these times. Here, we show that terahertz spectroscopy can directly investigate hydration layers. By a precise measurement of absorption coefficients between 2.3 THz and 2.9 THz we could determine the size and the characteristics of the hydration shell. The hydration layer around a carbohydrate (lactose) is determined to extend to 5.13 +/- 0.24 A from the surface corresponding to approximately 123 water molecules beyond the first solvation shell. Accompanying molecular modeling calculations support this result and provide a microscopic visualization. Terahertz spectroscopy is shown to probe the collective modes in the water network. The observed increase of the terahertz absorption of the water in the hydration layer is explained in terms of coherent oscillations of the hydration water and solute. Simulations also reveal a slowing down of the hydrogen bond rearrangement dynamics for water molecules near lactose, which occur on the picosecond time scale. The present study demonstrates that terahertz spectroscopy is a sensitive tool to detect solute-induced changes in the water network.
溶质周围水的动力学在化学和生物学中具有至关重要的意义。生物分子表面附近水分子的性质一直是众多实验和理论研究的主题,这些研究有时存在争议,一些研究表明在碳水化合物和蛋白质周围存在相当刚性的水结构[Pal, S. K., Peon, J., Bagchi, B. 和 Zewail A. H. (2002) J. Phys. Chem. B 106, 12376 - 12395]。水中氢键的重排在皮秒时间尺度上发生,因此相关实验必须能达到这些时间尺度。在这里,我们表明太赫兹光谱可以直接研究水合层。通过精确测量2.3太赫兹至2.9太赫兹之间的吸收系数,我们可以确定水合壳的大小和特征。确定围绕碳水化合物(乳糖)的水合层从表面延伸至5.13±0.24埃,这相当于超出第一溶剂化层约123个水分子。伴随的分子模型计算支持了这一结果,并提供了微观可视化。太赫兹光谱被证明可以探测水网络中的集体模式。水合层中水的太赫兹吸收增加是用水合水和溶质的相干振荡来解释的。模拟还揭示了乳糖附近水分子的氢键重排动力学在皮秒时间尺度上变慢。本研究表明太赫兹光谱是检测溶质引起的水网络变化的灵敏工具。