Schleucher Jürgen, Wijmenga Sybren S
Department of Medical Biochemistry and Biophysics, and Department of Organic Chemistry, Umeå University, S-90187 Umeå, Sweden.
J Am Chem Soc. 2002 May 22;124(20):5881-9. doi: 10.1021/ja012040o.
NOESY and ROESY cross-peak intensities depend on internuclear distances and internal motion. Internal motion is usually ignored, and NOESY cross-peak intensities are interpreted in terms of internuclear distances only. Off-resonance ROESY experiments measure a weighted average of NOE and ROE. The weight can be described and experimentally set by an angle theta;. For large enough molecules, NOE and ROE have opposite signs. Therefore, each cross-peak intensity becomes zero for an angle theta;(0). For any sample, the maximum angle theta;(0) is determined by the overall motion of the molecule. Smaller theta;(0) values reflect the angular component of internal motions. Because individual cross-peaks are analyzed, the method evaluates internal motions of individual H,H vectors. The reduction of theta;(0) is largest for internal motions on a time scale of 100-300 ps. The sensitivity of theta;(0) for internal motions decreases with increasing molecular weight. We estimate that detecting internal motions will be practicable for molecules up to about 15 kDa. We describe a protocol to measure theta;(0) from a series of off-resonance ROESY spectra. For such a series, we describe the choice of experimental parameters, a procedure to extract theta;(0) from the raw data, and the interpretation of theta;(0) in terms of internal motions. In the small protein BPTI, we analyzed 75 cross-peaks. The precision of theta;(0) was 0.25 degrees, as compared to typical reductions of theta;(0) of 3 degrees. We found a well-defined maximum theta;(0) for cross-peaks in rigid parts of the molecule, which reflects the overall motion of the molecule. For BPTI, also many structurally important long-range cross-peaks appear rigid. The lower theta;(0) values of long-range contacts involving methyl groups are consistent with methyl rotation on the 25-ps time scale. The lower theta;(0) values of the flexible C-terminus and of flexible side chains translate into upper limits for the angular order parameter of 0.4 and 0.5-0.8, respectively. Off-resonance ROESY can monitor internal motions of H,H contacts that are used in a structure calculation. Because no isotope labeling is needed, off-resonance ROESY can be used to detect internal motions in a wide range of natural products.
核Overhauser效应光谱(NOESY)和旋转核Overhauser效应光谱(ROESY)的交叉峰强度取决于核间距离和分子内部运动。分子内部运动通常被忽略,NOESY交叉峰强度仅根据核间距离进行解释。偏共振ROESY实验测量核Overhauser效应(NOE)和旋转核Overhauser效应(ROE)的加权平均值。权重可以用角度θ来描述并通过实验设定。对于足够大的分子,NOE和ROE具有相反的符号。因此,对于角度θ(0),每个交叉峰强度变为零。对于任何样品,最大角度θ(0)由分子的整体运动决定。较小的θ(0)值反映了分子内部运动的角度分量。由于对单个交叉峰进行分析,该方法评估单个H,H向量的内部运动。对于时间尺度为100 - 300皮秒(ps)的内部运动,θ(0)的降低最大。θ(0)对内部运动的灵敏度随分子量增加而降低我们估计对于分子量约达15 kDa的分子,检测内部运动是可行的。我们描述了一种从一系列偏共振ROESY光谱测量θ(0)的方案。对于这样一系列光谱,我们描述了实验参数的选择、从原始数据中提取θ(0)的程序以及根据内部运动对θ(0)进行的解释。在小蛋白抑肽酶(BPTI)中,我们分析了75个交叉峰。θ(0)的精度为0.25度,相比之下,θ(0)的典型降低值为3度。我们发现分子刚性部分的交叉峰有明确的最大θ(0),这反映了分子的整体运动。对于BPTI,许多在结构上重要的长程交叉峰似乎也是刚性的。涉及甲基的长程接触的较低θ(0)值与甲基在25皮秒时间尺度上的旋转一致。柔性C末端和柔性侧链的较低θ(0)值分别转化为角序参数的上限0.4和0.5 - 0.8。偏共振ROESY可以监测结构计算中使用的H,H接触的内部运动。由于不需要同位素标记,偏共振ROESY可用于检测多种天然产物中的内部运动。