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Solute-induced retardation of water dynamics probed directly by terahertz spectroscopy

机译:太赫兹光谱法直接探测溶质诱导的水动力学阻滞

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摘要

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. & 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 Å from the surface corresponding to ≈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.
机译:围绕溶质的水动力学在化学和生物学中至关重要。生物分子表面附近水分子的性质已成为众多(有时是有争议的)实验和理论研究的主题,其中一些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,SK,Peon,J. ,Bagchi,B。和Zewail AH(2002)J. Phys。化学B 106,12376–12395]。水中的氢键重排发生在皮秒级的时间范围内,因此相关的实验必须进入这些时间。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 THz至2.9 THz之间的吸收系数,我们可以确定水合壳的大小和特性。碳水化合物(乳糖)周围的水合层被确定从对应于≈123个水分子的表面超出第一个溶剂化壳延伸至5.13±0.24Å。伴随的分子建模计算支持该结果并提供微观可视化。太赫兹光谱显示出探测水网络中的集体模式。用水化水和溶质的相干振荡解释了水合层中水的太赫兹吸收的增加。模拟还揭示了在皮秒级时发生的乳糖附近水分子氢键重排动力学的减慢。本研究表明太赫兹光谱法是检测水网络中溶质引起的变化的灵敏工具。

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