Stanley Christopher, Rau Donald C
Neutron Scattering Science Division, Oak Ridge National Laboratory, PO Box 2008 MSC 6473, Oak Ridge, TN 37831.
Curr Opin Colloid Interface Sci. 2011 Dec;16(6):551-556. doi: 10.1016/j.cocis.2011.04.010.
Structured water on apposing surfaces can generate significant energies due to reorganization and displacement of water as the surfaces encounter each other. Force measurements on a multitude of biological structures using the osmotic stress technique have elucidated commonalities that point toward an underlying hydration force. In this review, the forces of two contrasting systems are considered in detail: highly charged DNA and nonpolar, uncharged hydroxypropyl cellulose. Conditions for both net repulsion and attraction, along with the measured exclusion of chemically different solutes from these macromolecular surfaces, are explored and demonstrate common features consistent with a hydration force origin. Specifically, the observed interaction forces can be reduced to the effects of perturbing structured surface water.
当相对的表面相互接触时,由于水的重新排列和位移,表面上的结构化水会产生显著的能量。使用渗透压技术对多种生物结构进行的力测量揭示了指向潜在水化力的共性。在这篇综述中,详细考虑了两个对比系统的力:高电荷的DNA和非极性、不带电荷的羟丙基纤维素。探讨了净排斥和吸引的条件,以及从这些大分子表面测量到的不同化学溶质的排斥情况,结果表明这些共同特征与水化力的起源一致。具体而言,观察到的相互作用力可归结为对结构化表面水的扰动效应。