Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Suita, Osaka 565-0871, Japan.
J Magn Reson. 2010 Apr;203(2):253-6. doi: 10.1016/j.jmr.2010.01.005. Epub 2010 Jan 15.
The combined use of selective deuteration, stereo-array isotope labeling (SAIL), and fast magic-angle spinning effectively suppresses the 1H-1H dipolar couplings in organic solids. This method provided the high-field 1H NMR linewidths comparable to those achieved by combined rotation and multiple-pulse spectroscopy. This technique was applied to two-dimensional 1H-detected 1H-1H polarization transfer CHH experiments of valine. The signal sensitivity for the 1H-detected CHH experiments was greater than that for the 13C-detected 1H-1H polarization transfer experiments by a factor of 2-4. We obtained the 1H-1H distances in SAIL valine by CHH experiments with an accuracy of about 0.2A by using a theory developed for 1H-1H polarization transfer in 13C-labeled organic compounds.
氘代与立体阵列同位素标记(SAIL)的联合使用,以及快速魔角旋转,有效地抑制了有机固体中的 1H-1H 偶极耦合。该方法提供了与通过联合旋转和多脉冲光谱学实现的高场 1H NMR 线宽相当的高场 1H NMR 线宽。该技术应用于缬氨酸的二维 1H 检测 1H-1H 极化转移 CHH 实验。通过 CHH 实验获得的 1H 检测 CHH 实验的信号灵敏度比 13C 检测 1H-1H 极化转移实验高 2-4 倍。我们通过对 13C 标记有机化合物中 1H-1H 极化转移理论的改进,通过 CHH 实验获得了 SAIL 缬氨酸的 1H-1H 距离,精度约为 0.2A。