Impact of urea on water structure: a clue to its properties as a denaturant?

被引:198
作者
Soper, AK [1 ]
Castner, EW
Luzar, A
机构
[1] Rutherford Appleton Lab, ISIS Dept, Didcot OX11 0QX, Oxon, England
[2] Rutgers State Univ, Dept Chem & Chem Biol, Piscataway, NJ 08854 USA
[3] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
neutron diffraction; isotope substitution; protein denaturation; hydration;
D O I
10.1016/S0301-4622(03)00095-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A new investigation of the Structure of urea-water solutions at a mole ratio of I urea to 4 water molecules is described. Neutron diffraction is used in conjunction with isotope labelling on the water and urea hydrogen atoms and on the nitrogen atom of urea. The diffraction data are analysed using the empirical potential structure refinement procedure to yield a set of site-site radial distribution functions and spatial density functions that are consistent with the diffraction data. The results are discussed in relation to recent and past X-ray and neutron diffraction experiments and theoretical studies of this system. It is found that urea incorporates readily into water, forming pronounced hydrogen bonds with water at both the amine and carbonyl headgroups. In addition the urea also hydrogen bonds to itself, forming chains or clusters consisting of up to approximately 60 urea molecules in a cluster. There, is however, little or no evidence of urea segregating itself from water, in marked contrast to a recent study of the methanol-water system. This behaviour is discussed in the context of the great propensity of urea to effect protein denaturation. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:649 / 666
页数:18
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