Fry D C, Kuby S A, Mildvan A S
Biochemistry. 1985 Aug 13;24(17):4680-94. doi: 10.1021/bi00338a030.
Proton NMR was used to study the interaction of beta,gamma-bidentate Cr3+ATP and MgATP with rabbit muscle adenylate kinase, which has 194 amino acids, and with a synthetic peptide consisting of residues 1-45 of the enzyme, which has previously been shown to bind MgepsilonATP [Hamada, M., Palmieri, R. H., Russell, G. A., & Kuby, S. A. (1979) Arch. Biochem. Biophys. 195, 155-177]. The peptide is globular and binds Cr3+ATP competitively with MgATP with a dissociation constant, KD(Cr3+ATP) = 35 microM, comparable to that of the complete enzyme [KI(Cr3+ATP) = 12 microM]. Time-dependent nuclear Overhauser effects (NOE's) were used to measure interproton distances on enzyme- and peptide-bound MgATP. The correlation time was measured directly for peptide-bound MgATP by studying the frequency dependence of the NOE's at 250 and 500 MHz. The H2' to H1' distance so obtained (3.07 A) was within the range established by X-ray and model-building studies of nucleotides (2.9 +/- 0.2 A). Interproton distances yielded conformations of enzyme- and peptide-bound MgATP with indistinguishable anti-glycosyl torsional angles (chi = 63 +/- 12 degrees) and 3'-endo/O1'-endo ribose puckers (sigma = 96 +/- 12 degrees). Enzyme- and peptide-bound MgATP molecules exhibited different C4'-C5' torsional angles (gamma) of 170 degrees and 50 degrees, respectively. Ten intermolecular NOE's from protons of the enzyme and four such NOE's from protons of the peptide to protons of bound MgATP were detected, which indicated proximity of the adenine ribose moiety to the same residues on both the enzyme and the peptide. Paramagnetic effects of beta,gamma-bidentate Cr3+ATP on the longitudinal relaxation rates of protons of the peptide provided a set of distances to the side chains of five residues, which allowed the location of the bound Cr3+ atom to be uniquely defined. Distances from enzyme-bound Cr3+ATP to the side chains of three residues of the protein agreed with those measured for the peptide. The mutual consistency of interproton and Cr3+ to proton distances obtained in metal-ATP complexes of both the enzyme and the peptide suggests that the conformation of the peptide is very similar to that of residues 1-45 of the enzyme. When this was assumed to be the case and when molecular models and a computer graphics system were used, MgATP could be fit into the X-ray structure of adenylate kinase in a unique manner such that all of the distances determined by NMR were accommodated.(ABSTRACT TRUNCATED AT 400 WORDS)
利用质子核磁共振(Proton NMR)研究了β,γ-双齿Cr³⁺-ATP和MgATP与兔肌腺苷酸激酶(含194个氨基酸)以及由该酶1 - 45位残基组成的合成肽之间的相互作用,此前已证明该合成肽能结合MgεATP [滨田,M.,帕尔米耶里,R. H.,拉塞尔,G. A.,& 库比,S. A.(1979年)《生物化学与生物物理学报》195, 155 - 177]。该肽呈球状,能与MgATP竞争性结合Cr³⁺-ATP,解离常数KD(Cr³⁺-ATP) = 35 μM,与完整酶的解离常数[KI(Cr³⁺-ATP) = 12 μM]相当。利用时间依赖性核Overhauser效应(NOE)来测量酶结合和肽结合的MgATP上的质子间距离。通过研究250和500 MHz下NOE的频率依赖性,直接测量了肽结合的MgATP的相关时间。由此获得的H2'至H1'距离(3.07 Å)在通过核苷酸的X射线和模型构建研究确定的范围内(2.9 ± 0.2 Å)。质子间距离产生了酶结合和肽结合的MgATP的构象,其反式糖基扭转角(χ = 63 ± 12°)和3'-内/ O1'-内核糖褶皱(σ = 96 ± 12°)难以区分。酶结合和肽结合的MgATP分子分别表现出170°和50°的不同C4'-C5'扭转角(γ)。检测到来自酶质子的10个分子间NOE以及来自肽质子的4个此类NOE与结合的MgATP的质子,这表明腺嘌呤核糖部分与酶和肽上的相同残基接近。β,γ-双齿Cr³⁺-ATP对肽质子纵向弛豫率的顺磁效应提供了到五个残基侧链的一组距离,从而能够唯一确定结合的Cr³⁺原子的位置。从酶结合的Cr³⁺-ATP到蛋白质三个残基侧链的距离与肽测量的距离一致。在酶和肽的金属-ATP复合物中获得的质子间以及Cr³⁺到质子的距离相互一致,表明该肽的构象与酶的1 - 45位残基的构象非常相似。当假设情况如此并使用分子模型和计算机图形系统时,MgATP可以以独特方式拟合到腺苷酸激酶的X射线结构中,使得NMR确定的所有距离都能得到满足。(摘要截取自400字)