Schmidt-Rohr Klaus, Hong Mei
Department of Chemistry, Iowa State University, Ames, Iowa 50011, USA.
J Am Chem Soc. 2003 May 14;125(19):5648-9. doi: 10.1021/ja0344415.
A new magic-angle spinning NMR method for measuring internuclear distances between a 13C-labeled site and amide protons is described. The magnetization of the protons evolves under homonuclear decoupling and the recoupled 13C-1H dipolar interaction, which provides simple spin-pair REDOR curves if only one 13C-labeled site is present. The modulation of the amide proton HN is detected via short 1H-15N cross polarization followed by 15N detection. The method is demonstrated on two specifically 13C- and 15N-labeled peptides, with 13C-HN distances from 2.2 to ca. 6 A. This technique promises to be particularly useful for measuring distances between 13C=O and H-15N groups, to identify hydrogen bonds in peptides and proteins.
本文描述了一种用于测量13C标记位点与酰胺质子之间核间距的新型魔角旋转核磁共振方法。质子的磁化在同核去耦和重新耦合的13C-1H偶极相互作用下演化,如果只存在一个13C标记位点,这会提供简单的自旋对旋转回波双共振(REDOR)曲线。通过短的1H-15N交叉极化随后进行15N检测来检测酰胺质子HN的调制。该方法在两种特定的13C和15N标记的肽上得到了验证,13C-HN距离在2.2至约6埃之间。这项技术有望在测量13C=O和H-15N基团之间的距离以识别肽和蛋白质中的氢键方面特别有用。