Gronenborn A M, Clore G M
Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
Biochemistry. 1989 Jul 11;28(14):5978-84. doi: 10.1021/bi00440a039.
The relative contributions of the interproton distance restraints derived from nuclear Overhauser enhancement measurements and of the empirical energy function in the determination of oligonucleotide structures by restrained molecular dynamics are investigated. The calculations are based on 102 intraresidue and 126 interresidue interproton distance restraints derived from short mixing time two-dimensional nuclear Overhauser enhancement data on the dodecamer 5'd(CGCGPATTCGCG)2 [Clore, G.M., Oschkinat, H., McLaughlin, L.W., Benseler, F., Scalfi Happ, C., Happ, E., & Gronenborn, A.M. (1988) Biochemistry 27, 4185-4197]. Eight interproton distance restraint lists were made up with errors ranging from -0.1/+0.2 to -1.2/+1.3 A for r less than 2.5 A and from -0.2/+0.3 to -1.3/+1.4 A for r greater than or equal to 2.5 A. These restraints were incorporated into the total energy function of the system in the form of square-well potentials with force constants set sufficiently high to ensure that the deviations between calculated distances and experimental restraints were very small (average interproton distance rms deviation of less than 0.06 A). For each data set, six calculations were carried out, three starting from classical A-DNA and three from classical B-DNA. The results show that structural changes occurring during the course of restrained molecular dynamics and the degree of structural convergence are determined by the interproton distance restraints. All the structures display similar small deviations from idealized geometry and have the same values for the nonbonding energy terms comprising van der Waals, electrostatic, and hydrogen-bonding components. Thus, the function of the empirical energy function is to maintain near perfect stereochemistry and nonbonded interactions.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了在通过受限分子动力学确定寡核苷酸结构时,源自核Overhauser增强测量的质子间距离约束和经验能量函数的相对贡献。计算基于从十二聚体5'd(CGCGPATTCGCG)2的短混合时间二维核Overhauser增强数据得出的102个残基内和126个残基间质子间距离约束[Clore, G.M., Oschkinat, H., McLaughlin, L.W., Benseler, F., Scalfi Happ, C., Happ, E., & Gronenborn, A.M. (1988) Biochemistry 27, 4185 - 4197]。构建了八个质子间距离约束列表,对于r小于2.5 Å,误差范围为 -0.1/+0.2至 -1.2/+1.3 Å;对于r大于或等于2.5 Å,误差范围为 -0.2/+0.3至 -1.3/+1.4 Å。这些约束以方阱势的形式纳入系统的总能量函数中,力常数设置得足够高,以确保计算距离与实验约束之间的偏差非常小(平均质子间距离均方根偏差小于0.06 Å)。对于每个数据集,进行了六次计算,三次从经典A - DNA开始,三次从经典B - DNA开始。结果表明,在受限分子动力学过程中发生的结构变化和结构收敛程度由质子间距离约束决定。所有结构与理想化几何形状的偏差都很小,并且在包括范德华、静电和氢键成分的非键能项上具有相同的值。因此,经验能量函数的作用是维持近乎完美的立体化学和非键相互作用。(摘要截断于250字)