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通过中子散射、X 射线衍射和 DSC 的组合观察细微的动态转变:以单斜 L-半胱氨酸为例。

Observation of subtle dynamic transitions by a combination of neutron scattering, X-ray diffraction and DSC: a case study of the monoclinic L-cysteine.

机构信息

Helmholtz-Zentrum Berlin für Materialien und Energie, Hahn-Meitner Platz, 1 14109 Berlin, Germany.

出版信息

Biophys Chem. 2010 May;148(1-3):34-41. doi: 10.1016/j.bpc.2010.02.003. Epub 2010 Feb 11.

Abstract

The paper illustrates the benefit of combining several experimental techniques (incoherent elastic and inelastic neutron scattering, DSC, and X-ray diffraction) to study subtle dynamic transitions in a biologically important system, probing a broad time (frequency) range of the molecular motions in a wide temperature interval of 2-300K. As a case study the crystalline form (a monoclinic polymorph) of l-cysteine ((+)NH(3)-CH(CH(2)SH)-COO(-)) - an essential amino acid - has been selected. Crystals of amino acids are widely used to mimic important structural and dynamic features of peptides. The conformational lability of cysteine and the dynamics of the thiol-side chains are known to account for various phase transitions in the crystalline state and for the conformational transitions important for the biological function in the peptides. The effect of temperature on the monoclinic polymorph of l-cysteine, metastable at ambient conditions, has been studied for the first time. A dynamical transition at about 150K, marking a crossover of the molecular fluctuations between harmonic and non-harmonic dynamical regimes, was evidenced by evaluating the evolution of the mean-square displacement obtained from the elastic fixed window approach using the backscattering spectrometer IN10 located at the ILL. Although this transition does not manifest itself in the DSC, it was clearly observed by incoherent inelastic neutron scattering. By analyzing the dynamical susceptibility contribution (chi''(omega)) obtained using IN6 also at ILL we were able to evidence another relaxation process at a different time scale. The disordered soft l-cysteine structure has an excess of inelastic scattering at about 3meV, analogous to the "boson peak" observed in glass-like materials and proteins. High-precision X-ray diffraction has revealed an anomaly in the changes of selected unit cell parameters and volume at about 240K.

摘要

本文阐述了将几种实验技术(非相干弹性和非弹性中子散射、差示扫描量热法和 X 射线衍射)结合起来研究生物体系中微妙动态转变的优势,该体系可以在 2-300K 的宽温度范围内探测分子运动的宽频(时)域。作为案例研究,选择了(+)NH(3)-CH(CH(2)SH)-COO(-)形式的 l-半胱氨酸(一种必需氨基酸)的晶型(单斜多晶型)。氨基酸晶体被广泛用于模拟肽的重要结构和动态特征。众所周知,半胱氨酸的构象不稳定性和巯基侧链的动力学导致了晶体状态中的各种相变,以及对肽中生物功能很重要的构象转变。首次研究了在环境条件下亚稳存在的 l-半胱氨酸单斜多晶型对温度的影响。通过评估从 IN10 背散射光谱仪位于 ILL 的弹性固定窗口方法获得的均方根位移的演化,证明了在大约 150K 处存在分子波动从调和到非调和动力学状态的交叉的动力学转变。尽管该转变在差示扫描量热法中没有表现出来,但在非相干非弹性中子散射中可以清楚地观察到。通过分析也在 ILL 处的 IN6 获得的动态磁化率贡献(chi''(omega)),我们能够证明在不同的时间尺度上存在另一个弛豫过程。无序软 l-半胱氨酸结构在大约 3meV 处具有过剩的非弹性散射,类似于玻璃状材料和蛋白质中观察到的“声子峰”。高精密 X 射线衍射揭示了在大约 240K 时,所选晶胞参数和体积的变化出现异常。

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