Paci M, Pon C, Lammi M, Gualerzi C
J Biol Chem. 1984 Aug 10;259(15):9628-34.
Translational initiation factor-3 (IF-3) was characterized by 1H NMR spectroscopy as a function of pH and temperature and following chemical modifications. Spin-lattice relaxation times for individual resonances and bands were also measured. Several resonances were assigned to different amino acid residues by different criteria. Among these are the CH3-N of the N-terminal methionine which appears free, mobile, and very sensitive to the modification of several physicochemical parameters as well as the 3,5 and 2,6 protons of the three tyrosines (two of which play a role in the function of IF-3) which were found to be located in different magnetic environments. Two of these residues appear to be close to each other and in the vicinity of a slow reacting arginine within the tertiary structure of the factor. The properties and the titration behavior of the imidazole proton resonances suggest that the single His residue is partially buried in the protein structure. Characteristic of the IF-3 spectrum also is the presence of an abundant subset of Arg delta-CH2, Lys epsilon-CH2, and CH3 protons displaying clear cut upfield perturbations. These are probably due to the coming together of two or more apolar "fronts" which possibly arise from distant parts of the molecule and result in the close proximity between aromatic rings and aliphatic side chains. The IF-3 spectrum also includes several distinct methyl resonances significantly shifted upfield by aromatic ring currents. Overall, the characteristics of the spectrum, its relative insensitivity to temperature and ionic strength, and the existence of extensive cross-relaxation phenomena indicate that IF-3 has a highly folded tertiary structure with abundant hydrophobic regions. In spite of some heterogeneity in the distribution of the side chain environments, no indication was found for the existence of distinct domains or, at least, of extensive regions with higher mobility.
通过1H NMR光谱对翻译起始因子-3(IF-3)进行了表征,研究了其作为pH值、温度以及化学修饰的函数关系。还测量了各个共振峰和谱带的自旋晶格弛豫时间。通过不同标准将几个共振峰归属于不同的氨基酸残基。其中包括N端甲硫氨酸的CH3-N,它表现为自由、可移动,并且对几个物理化学参数的变化非常敏感;还有三个酪氨酸的3,5和2,6质子(其中两个在IF-3的功能中起作用),它们处于不同的磁性环境中。其中两个残基似乎彼此靠近,并且在该因子三级结构中一个反应较慢的精氨酸附近。咪唑质子共振的性质和滴定行为表明,单个组氨酸残基部分埋藏在蛋白质结构中。IF-3光谱的特征还包括存在大量的精氨酸δ-CH2、赖氨酸ε-CH2和CH3质子子集,它们显示出明显的向上场扰动。这可能是由于两个或更多非极性“前沿”聚集在一起,这些前沿可能源自分子的远处部分,导致芳香环和脂肪族侧链紧密靠近。IF-3光谱还包括几个明显因芳香环电流而向上场显著位移的不同甲基共振峰。总体而言,光谱的特征、其对温度和离子强度的相对不敏感性以及广泛交叉弛豫现象的存在表明,IF-3具有高度折叠的三级结构,且有丰富的疏水区域。尽管侧链环境分布存在一些异质性,但未发现存在明显结构域的迹象,或者至少未发现存在具有更高流动性的广泛区域的迹象。