Blake P R, Park J B, Bryant F O, Aono S, Magnuson J K, Eccleston E, Howard J B, Summers M F, Adams M W
Department of Chemistry and Biochemistry, University of Maryland Baltimore County 21228.
Biochemistry. 1991 Nov 12;30(45):10885-95. doi: 10.1021/bi00109a012.
The purification, amino acid sequence, and two-dimensional 1H NMR results are reported for the rubredoxin (Rd) from the hyperthermophilic archaebacterium Pyrococcus furiosus, an organism that grows optimally at 100 degrees C. The molecular mass (5397 Da), iron content (1.2 +/- 0.2 g-atom of Fe/mol), UV-vis spectrophotometric properties, and amino acid sequence (60% sequence identity with Clostridium pasteurianum Rd) are found to be typical of this class of redox protein. However, P. furiosus Rd is remarkably thermostable, being unaffected after incubation for 24 h at 95 degrees C. One- and two-dimensional 1H nuclear magnetic resonance spectra of the oxidized [Fe(III)Rd] and reduced [Fe(II)Rd] forms of P. furiosus Rd exhibited substantial paramagnetic line broadening, and this precluded detailed 3D structural studies. The apoprotein was not readily amenable to NMR studies due to apparent protein oxidation involving the free cysteine sulfhydryls. However, high-quality NMR spectra were obtained for the Zn-substituted protein, Zn(Rd), enabling detailed NMR signal assignment for all backbone amide and alpha and most side-chain protons. Secondary structural elements were determined from qualitative analysis of 2D Overhauser effect spectra. Residues A1-K6, Y10-E14, and F48-E51 form a three-strand antiparallel beta-sheet, which comprises ca. 30% of the primary sequence. Residues C5-Y10 and C38-A43 form types I and II amide-sulfur tight turns common to iron-sulfur proteins. These structural elements are similar to those observed by X-ray crystallography for native Rd from the mesophile C. pasteurianum. However, the beta-sheet domain in P. furiosus Rd is larger than that in C. pasteurianum Rd and appears to begin at the N-terminal residue. From analysis of the secondary structure, potentially stabilizing electrostatic interactions involving the charged groups of residues Ala(1), Glu(14), and Glu(52) are proposed. These interactions, which are not present in rubredoxins from mesophilic organisms, may prevent the beta-sheet from "unzipping" at elevated temperatures.
报道了来自嗜热古细菌激烈火球菌的红氧还蛋白(Rd)的纯化、氨基酸序列和二维¹H NMR结果,激烈火球菌在100℃时生长最佳。发现其分子量(5397 Da)、铁含量(1.2±0.2克原子铁/摩尔)、紫外可见分光光度性质以及氨基酸序列(与巴氏梭菌Rd的序列同一性为60%)是这类氧化还原蛋白的典型特征。然而,激烈火球菌Rd具有显著的热稳定性,在95℃孵育24小时后不受影响。激烈火球菌Rd的氧化态[Fe(III)Rd]和还原态[Fe(II)Rd]形式的一维和二维¹H核磁共振谱显示出大量顺磁线展宽,这使得详细的三维结构研究无法进行。由于涉及游离半胱氨酸巯基的明显蛋白质氧化,脱辅基蛋白不易用于NMR研究。然而,获得了锌取代蛋白Zn(Rd)的高质量NMR谱,能够对所有主链酰胺以及α和大多数侧链质子进行详细的NMR信号归属。通过二维Overhauser效应谱的定性分析确定了二级结构元件。残基A¹-K⁶、Y¹⁰-E¹⁴和F⁴⁸-E⁵¹形成一个三股反平行β-折叠,约占一级序列的30%。残基C⁵-Y¹⁰和C³⁸-A⁴³形成铁硫蛋白常见的I型和II型酰胺-硫紧密转角。这些结构元件与通过X射线晶体学观察到的嗜温菌巴氏梭菌天然Rd的结构元件相似。然而,激烈火球菌Rd中的β-折叠结构域比巴氏梭菌Rd中的大,并且似乎从N端残基开始。通过对二级结构的分析,提出了涉及残基Ala(¹)、Glu(¹⁴)和Glu(⁵²)带电基团的潜在稳定静电相互作用。这些相互作用在嗜温生物的红氧还蛋白中不存在,可能会防止β-折叠在高温下“解开”。