Gronenborn A M, Bax A, Wingfield P T, Clore G M
Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD 20892.
FEBS Lett. 1989 Jan 16;243(1):93-8. doi: 10.1016/0014-5793(89)81224-4.
A powerful method of sequential resonance assignment of protein 1H-NMR spectra is presented and illustrated with respect to the DNA-binding protein ner from phage Mu. It is based on correlating proton-proton through-space and through-bond connectivities with the chemical shift of the directly bonded 15N atom. By this means, ambiguities arising from chemical shift degeneracy of amide proton resonances can be resolved. The experiments described involve combining the 1H-detected heteronuclear multiple quantum coherence correlation experiment with homonuclear nuclear Overhauser enhancement, J-correlated or Hartmann-Hahn experiments.
本文介绍了一种用于蛋白质1H-NMR谱序列共振归属的强大方法,并以噬菌体Mu的DNA结合蛋白ner为例进行说明。该方法基于将质子-质子的空间和键连相关性与直接相连的15N原子的化学位移相关联。通过这种方式,可以解决酰胺质子共振化学位移简并引起的模糊性。所描述的实验包括将1H检测的异核多量子相干相关实验与同核核Overhauser增强、J相关或Hartmann-Hahn实验相结合。