Yamasaki K, Muto Y, Ito Y, Wälchli M, Miyazawa T, Nishimura S, Yokoyama S
Department of Biophysics and Biochemistry, Faculty of Science, University of Tokyo, Japan.
J Biomol NMR. 1992 Jan;2(1):71-82. doi: 10.1007/BF02192801.
A 1H-15N NMR study was performed on the GDP-bound form of a truncated human c-Ha-ras oncogene product (171 amino acid residues). Resonance cross peaks of the backbone amide 1H-15N nuclei of a uniformly 15N-labeled protein were observed with heteronuclear single-quantum coherence spectroscopy (HSQC). In order to resolve overlapping cross peaks, selective 15N-labeling of one or two types of amino acid residues (Ala, Arg, Asx, Glx, Gly, His, Ile, Leu, Lys, Met, Phe, Ser, Thr, Tyr and/or Val) was carried out using appropriate E. coli mutant strains. By this procedure, all the backbone 1H-15N cross peaks were classified into amino acid types.
对截短的人c-Ha-ras癌基因产物(171个氨基酸残基)的GDP结合形式进行了1H-15N核磁共振研究。使用异核单量子相干光谱法(HSQC)观察到均匀15N标记蛋白质的主链酰胺1H-15N核的共振交叉峰。为了解析重叠的交叉峰,使用合适的大肠杆菌突变菌株对一两种氨基酸残基(丙氨酸、精氨酸、天冬氨酸、谷氨酸、甘氨酸、组氨酸、异亮氨酸、亮氨酸、赖氨酸、甲硫氨酸、苯丙氨酸、丝氨酸、苏氨酸、酪氨酸和/或缬氨酸)进行了选择性15N标记。通过该程序,所有主链1H-15N交叉峰都被分类为氨基酸类型。