Stein V M, Bond J P, Capp M W, Anderson C F, Record M T
Department of Chemistry, University of Wisconsin-Madison 53706, USA.
Biophys J. 1995 Mar;68(3):1063-72. doi: 10.1016/S0006-3495(95)80281-X.
The local cation concentration at the surface of oligomeric or polymeric B-DNA is expected, on the basis of MC simulations (Olmsted, M. C., C. F. Anderson, and M. T. Record, Jr. 1989. Proc. Natl. Acad. Sci. USA. 86:7766-7770), to decrease sharply as either end of the molecule is approached. In this paper we report 23Na NMR measurements indicating the importance of this "coulombic" end effect on the average extent of association of Na+ with oligomeric duplex DNA. In solutions containing either 20-bp synthetic DNA or 160-bp mononucleosomal calf thymus DNA at phosphate monomer concentrations [P] of 4-10 mM, measurements were made over the range of ratios 1 < or = [Na]/[LP] < or = 20, corresponding to Na+ concentrations of 4-200 nM. The longitudinal 23Na NMR relaxation rates measured in these NaDNA solutions, Robs, are interpreted as population-weighted averages of contributions from "bound" (RB) and "free" (RF) 23Na relaxation rates. The observed enhancements of Robs indicate that RB significantly exceeds RF, which is approximately equal to the 23Na relaxation rate in an aqueous solution containing only NaCl. Under salt-fre-tconditions ([Na]/[P] = 1), where the enhancement in Robs is maximal, we find that Robs--RF in the solution containing 160-bp DNA is approximately 1.8 times that observed for the 20-bp DNA. For the 160-bp oligomer (which theoretical calculations predict to be effectively polyion-like), we find that a plot of Robs v. [P]/[Na] is linear, as observed previously for sonicated (approximately 700 bp) DNA samples. For the 20-bp oligonucleotide this plot exhibits a marked departure from linearity that can be fitted to a quadratic function of [P]/[Na]. Monte Carlo simulations based on a simplified model are capable of reproducing the qualitative trends in the 23Na NMR measurements analyzed here. In particular, the dependences of Robs--RF on DNA charge magnitude of Z(320 vs. 38 phosphates) and (for the 20-bp oligomer) on [Na]/[P] are well correlated with the calculated average surface concentration of Na+. Thus, effects of sodium concentration on RB appear to be of secondary importance. We conclude that 23Na NMR relaxation measurements are a sensitive probe of the effects of oligomer charge on the extent of ion accumulation near B-DNA oligonucleotides, as a function of [Na] and [P].
基于蒙特卡罗模拟(奥姆斯特德,M. C.,C. F. 安德森,和 M. T. 雷科德,Jr. 1989. 《美国国家科学院院刊》. 86:7766 - 7770),预计寡聚或多聚 B - DNA 表面的局部阳离子浓度会随着分子两端的接近而急剧下降。在本文中,我们报告了 23Na 核磁共振测量结果,表明这种“库仑”端效应对于 Na+与寡聚双链 DNA 平均结合程度的重要性。在含有 20 个碱基对的合成 DNA 或 160 个碱基对的单核小体小牛胸腺 DNA 的溶液中,磷酸单体浓度[P]为 4 - 10 mM,在 1 ≤ [Na]/[LP] ≤ 20 的比例范围内进行测量,对应 Na+浓度为 4 - 200 nM。在这些 NaDNA 溶液中测量的纵向 23Na 核磁共振弛豫率 Robs,被解释为“结合”(RB)和“自由”(RF)23Na 弛豫率贡献的总体加权平均值。观察到的 Robs 增强表明 RB 显著超过 RF,RF 大约等于仅含 NaCl 的水溶液中的 23Na 弛豫率。在无盐条件下([Na]/[P] = 1),此时 Robs 的增强最大,我们发现在含有 160 个碱基对 DNA 的溶液中 Robs - RF 大约是含有 20 个碱基对 DNA 时观察值的 1.8 倍。对于 160 个碱基对的寡聚物(理论计算预测其实际上类似聚离子),我们发现 Robs 对[P]/[Na]的曲线是线性的,这与之前对超声处理的(约 700 个碱基对)DNA 样品的观察结果一致。对于 20 个碱基对的寡核苷酸,该曲线明显偏离线性,可以拟合为[P]/[Na]的二次函数。基于简化模型的蒙特卡罗模拟能够重现此处分析的 23Na 核磁共振测量中的定性趋势。特别是,Robs - RF 对 DNA 电荷大小 Z(320 个与 38 个磷酸基团)以及(对于 20 个碱基对的寡聚物)对[Na]/[P]的依赖性与计算出的 Na+平均表面浓度具有良好的相关性。因此,钠浓度对 RB 的影响似乎是次要的。我们得出结论,23Na 核磁共振弛豫测量是寡聚物电荷对 B - DNA 寡核苷酸附近离子积累程度影响的敏感探针,它是[Na]和[P]的函数。