Kiriukhin Michael Y, Collins Kim D
Department of Biochemistry and Molecular Biology, University of Maryland Medical School, Baltimore, MD 21201-1503, USA.
Biophys Chem. 2002 Oct 16;99(2):155-68. doi: 10.1016/s0301-4622(02)00153-9.
The role of ionized groups in biological systems is determined by their affinity for water [Biophys. J. 72 (1997) 65-76]. The tightly bound water associated with biologically important ions increases their apparent size. We define the apparent dynamic hydration number of an ion here as the number of tightly bound water molecules that must be assigned to the ion to explain its apparent molecular weight on a Sephadex G-10 size exclusion column, and report the first accurate determination of tightly bound water for 23 ions of biological significance, including H(+) and HO(-). We also calculate the radius of the equivalent hydrated sphere (r(h)) for each ion. We find that the ratio of the hydrated volumes of two ions approximates the ratio of the square of the charges of the same two ions. Since the 'ionic strength' of the solution also depends upon the square of the charges on the ions, our results suggest that ionic strength effects may largely arise from local effects related to the hydrated volume of the ion--that is, from space filling, osmotic, water activity, surface tension and hydration shell overlap effects rather than from long-range electric field effects.
生物系统中离子化基团的作用取决于它们对水的亲和力[《生物物理学杂志》72(1997)65 - 76]。与具有生物学重要性的离子紧密结合的水增加了它们的表观尺寸。我们在此将离子的表观动态水合数定义为为解释其在葡聚糖G - 10尺寸排阻柱上的表观分子量而必须分配给该离子的紧密结合水分子的数量,并报告了对包括H⁺和OH⁻在内的23种具有生物学意义的离子的紧密结合水的首次精确测定结果。我们还计算了每种离子的等效水合球体半径(rₕ)。我们发现,两种离子的水合体积之比近似于这两种离子电荷平方之比。由于溶液的“离子强度”也取决于离子上电荷的平方,我们的结果表明,离子强度效应可能主要源于与离子水合体积相关的局部效应——即源于空间填充、渗透、水活性、表面张力和水合壳重叠效应,而非源于长程电场效应。