Post C B
Department of Medicinal Chemistry, Purdue University, West Lafayette, IN 47907.
J Mol Biol. 1992 Apr 20;224(4):1087-101. doi: 10.1016/0022-2836(92)90471-u.
Dynamic averaging effects from internal motions on interproton distances estimated from nuclear Overhauser effects (NOE) are determined by using a molecular dynamics simulation of lysozyme. Generalized order parameters measuring angular averaging and radial averaging parameters are calculated. The product of these two parameters describes the full averaging effects on cross-relaxation. Analysis of 2778 non-methyl NOE interactions from the protein interior and surface indicates that distances estimated by assuming a rigid molecule have less than 10% error for 89% of the NOE interactions. However, analysis of 1854 methyl interactions found that only 68% of the distances estimated from cross-relaxation rates would have less than 10% error. Qualitative evaluation of distances according to strong, medium and weak NOE intensities, when used to define only the upper bound for interproton separation, would misassign less than 1% of the distance constraints because of motional averaging. Internal motions do not obscure the identification of secondary structure, although some instances of significant averaging effects were found for interactions in alpha-helical regions. Interresidue NOEs for amino acids more than three residues apart in the primary sequence are more extensively averaged than intraresidue or short-range interresidue NOEs. Intraresidue interactions exhibit a greater degree of angular averaging than those involving interresidue proton pairs. An internal motion does not equally affect all NOE interactions for a particular proton. Thus, incorporation of averaging parameters in nuclear magnetic resonance structure determination procedures must be made on a proton-pair-wise basis. On the basis of the motional averaging results, particular fixed-distance proton pairs in proteins are suggested for use as distance references. A small percentage of NOE pairs localized to three regions of the protein exhibit extreme averaging effects from internal motions. The regions and types of motions involved are described.
通过对溶菌酶进行分子动力学模拟,确定了内部运动对由核Overhauser效应(NOE)估算的质子间距离产生的动态平均效应。计算了测量角度平均的广义序参数和径向平均参数。这两个参数的乘积描述了对交叉弛豫的完整平均效应。对来自蛋白质内部和表面的2778个非甲基NOE相互作用的分析表明,对于89%的NOE相互作用,假设分子刚性时估算的距离误差小于10%。然而,对1854个甲基相互作用的分析发现,从交叉弛豫率估算的距离中只有68%的误差小于10%。根据强、中、弱NOE强度对距离进行定性评估,当仅用于定义质子间分离的上限时,由于运动平均,距离约束的错误分配不到1%。内部运动不会模糊二级结构的识别,尽管在α-螺旋区域的相互作用中发现了一些显著平均效应的实例。一级序列中相隔三个以上残基的氨基酸之间的残基间NOE比残基内或短程残基间NOE的平均程度更高。残基内相互作用比涉及残基间质子对的相互作用表现出更大程度的角度平均。内部运动不会对特定质子的所有NOE相互作用产生同等影响。因此,在核磁共振结构测定程序中纳入平均参数必须基于质子对逐一进行。根据运动平均结果,建议将蛋白质中特定的固定距离质子对用作距离参考。一小部分定位于蛋白质三个区域的NOE对表现出内部运动产生的极端平均效应。描述了所涉及的区域和运动类型。