Dubs A, Wagner G, Wüthrich K
Biochim Biophys Acta. 1979 Mar 27;577(1):177-94. doi: 10.1016/0005-2795(79)90020-5.
Studies of proton-proton nuclear Overhauser effects were used to obtain individual assignments of 17 amide proton resonances in the 360 MHz proton nuclear magnetic resonance spectrum of the basic pancreatic trypsin inhibitor. First, optimizing the conditions for obtaining selective nuclear Overhauser effects in the presence of spin diffusion in macromolecules is discussed. Truncated driven nuclear Overhauser experiments were used to assing the amide proton resonances of the beta-sheet in the inhibitor. It is suggested that these techniques could serve quite generally to obtain individual resonance assignments in beta-sheet secondary structures of proteins. Combination of nuclear Overhauser studies with spin decoupling further resulted in individual assignments of the gamma-methyl resonances of the two isoleucines and numerous Calpha and Cbeta protons.
利用质子-质子核Overhauser效应的研究,对碱性胰蛋白酶抑制剂在360兆赫质子核磁共振谱中的17个酰胺质子共振进行了单独归属。首先,讨论了在大分子存在自旋扩散的情况下优化获得选择性核Overhauser效应的条件。截断驱动核Overhauser实验被用于确定抑制剂中β-折叠的酰胺质子共振。有人提出,这些技术一般可用于获得蛋白质β-折叠二级结构中的单个共振归属。核Overhauser研究与自旋去耦相结合,进一步实现了两个异亮氨酸的γ-甲基共振以及众多α-碳和β-碳质子的单独归属。