Hu J S, Bax A
Laboratory of Chemical Physics, National Institutes of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0520, USA.
J Biomol NMR. 1997 Apr;9(3):323-8. doi: 10.1023/a:1018691228238.
New quantitative J correlation experiments are used for measuring all two- and three-bond couplings between 15N and aliphatic side-chain carbons in proteins uniformly enriched in 13C and 15N. Results show that 3JNC beta and 2JNC beta invariably are very small. Therefore, a simple and relatively sensitive two-dimensional spin-echo difference experiment can be used to identify residues with a 3JN gamma coupling substantially larger than 1 Hz, indicative of a trans arrangement between N and C gamma. This measurement therefore provides chi 1 angle information for residues with an aliphatic C gamma carbon, and thereby also aids in making stereospecific assignments of H beta resonances. Experiments are demonstrated for ubiquitin and for a complex between calmodulin and a 26-residue peptide.
新的定量J相关实验用于测量均匀富集13C和15N的蛋白质中15N与脂肪族侧链碳之间的所有二键和三键耦合。结果表明,3JNCβ和2JNCβ始终非常小。因此,一个简单且相对灵敏的二维自旋回波差异实验可用于识别具有远大于1Hz的3JNγ耦合的残基,这表明N和Cγ之间为反式排列。因此,该测量为具有脂肪族Cγ碳的残基提供了χ1角信息,从而也有助于对Hβ共振进行立体特异性归属。针对泛素以及钙调蛋白与一个26个残基的肽之间的复合物进行了实验演示。