Campbell-Burk S
Department of Biochemistry, Brandeis University, Waltham, Massachusetts 02254.
Biochemistry. 1989 Nov 28;28(24):9478-84. doi: 10.1021/bi00450a035.
[15N]Glycine was biosynthetically incorporated into normal cellular N-ras p21 and a position 12 transforming mutant, in order to produce p21 proteins containing several site-specific NMR probes at or near activating positions in the guanine nucleotide binding domain. We have previously assigned all five glycine resonances located in loops directly involved in binding of guanosine diphosphate in the wild-type p21 protein [Campbell-Burk, S., Papastavros, M. Z., McCormick, F., & Redfield, A. G. (1989) Proc. Natl. Acad. Sci. U.S.A 86, 817-820]. In this report, the corresponding glycine resonances in the p21 mutant have been assigned, and spectral differences between normal and mutant p21-guanosine diphosphate (p21.GDP) complexes have been investigated. Our combined 1H[15N] and 31P NMR results show that substitution of aspartate for glycine-12 produces perturbations in the phosphoryl binding domain, near the point of the mutation. Although many of the remaining glycines were unaffected, spectral differences were also observed outside the GDP binding domain. Two of the five active-site glycines in wild-type p21.GDP have very slow amide proton exchange rates with water (kappa less than 2.8 x 10(-5) s-1). The active-site glycines are located in solvent-exposed loops, so their apparent solvent inaccessibility may result from strong hydrogen bond formation between glycine amide protons and bound guanine diphosphate and/or other nearby groups in p21.
将[15N]甘氨酸通过生物合成的方式掺入正常细胞的N-ras p21及12位转化突变体中,以产生在鸟嘌呤核苷酸结合结构域的激活位点或其附近含有多个位点特异性核磁共振探针的p21蛋白。我们之前已归属了野生型p21蛋白中直接参与二磷酸鸟苷结合的环内的所有五个甘氨酸共振峰[坎贝尔 - 伯克,S.,帕帕斯塔夫罗斯,M. Z.,麦科密克,F.,& 雷德菲尔德,A. G.(1989年)《美国国家科学院院刊》86,817 - 820]。在本报告中,已归属了p21突变体中相应的甘氨酸共振峰,并研究了正常和突变型p21 - 二磷酸鸟苷(p21.GDP)复合物之间的光谱差异。我们结合的1H[15N]和31P核磁共振结果表明,将天冬氨酸取代甘氨酸 - 12会在突变位点附近的磷酰基结合结构域产生扰动。尽管其余许多甘氨酸未受影响,但在GDP结合结构域之外也观察到了光谱差异。野生型p21.GDP中五个活性位点甘氨酸中的两个与水的酰胺质子交换速率非常慢(κ小于2.8×10^(-5) s^(-1))。活性位点甘氨酸位于溶剂暴露的环中,因此它们明显难以接近溶剂可能是由于甘氨酸酰胺质子与结合的二磷酸鸟苷和/或p21中其他附近基团之间形成了强氢键。