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里氏木霉纤维二糖水解酶I C端结构域三维溶液结构的测定。一项利用核磁共振和混合距离几何-动力学模拟退火的研究。

Determination of the three-dimensional solution structure of the C-terminal domain of cellobiohydrolase I from Trichoderma reesei. A study using nuclear magnetic resonance and hybrid distance geometry-dynamical simulated annealing.

作者信息

Kraulis J, Clore G M, Nilges M, Jones T A, Pettersson G, Knowles J, Gronenborn A M

机构信息

Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892.

出版信息

Biochemistry. 1989 Sep 5;28(18):7241-57. doi: 10.1021/bi00444a016.

Abstract

The solution structure of a synthetic 36-residue polypeptide comprising the C-terminal cellulose binding domain of cellobiohydrolase I (CT-CBH I) from Trichoderma reesei was investigated by nuclear magnetic resonance (NMR) spectroscopy. The 1H NMR spectrum was completely assigned in a sequential manner by two-dimensional NMR techniques. A large number of stereospecific assignments for beta-methylene protons, as well as ranges for the phi, psi, and chi 1 torsion angles, were obtained on the basis of sequential and intraresidue nuclear Overhauser enhancement (NOE) and coupling constant data in combination with a conformational data base search. The structure calculations were carried out in an iterative manner by using the hybrid distance geometry-dynamical simulated annealing method. This involved computing a series of initial structures from a subset of the experimental data in order to resolve ambiguities in the assignments of some NOE cross-peaks arising from chemical shift degeneracy. Additionally, this permitted us to extend the stereospecific assignments to the alpha-methylene protons of glycine using information on phi torsion angles derived from the initial structure calculations. The final experimental data set consisted of 554 interproton distance restraints, 24 restraints for 12 hydrogen bonds, and 33 phi, 24 psi, and 25 chi 1 torsion angle restraints. CT-CBH I has two disulfide bridges whose pairing was previously unknown. Analysis of structures calculated with all three possible combinations of disulfide bonds, as well as without disulfide bonds, indicated that the correct disulfide bridge pairing was 8-25 and 19-35. Forty-one structures were computed with the 8-25 and 19-35 disulfide bridges, and the average atomic rms difference between the individual structures and the mean structure obtained by averaging their coordinates was 0.33 +/- 0.04 A for the backbone atoms and 0.52 +/- 0.06 A for all atoms. The protein has a wedgelike shape with an amphiphilic character, one face being predominantly hydrophilic and the other mainly hydrophobic. The principal element of secondary structure is made up of an irregular triple-stranded antiparallel beta-sheet composed of residues 5-9 (beta 1), 24-28 (beta 2), and 33-36 (beta 3) in which strand beta 3 is hydrogen bonded to the other two strands.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

利用核磁共振(NMR)光谱研究了一种合成的36个残基多肽的溶液结构,该多肽包含里氏木霉纤维二糖水解酶I(CT-CBH I)的C端纤维素结合结构域。通过二维NMR技术以序列方式完全归属了1H NMR谱。基于序列和残基内的核Overhauser效应(NOE)以及耦合常数数据,并结合构象数据库搜索,获得了大量β-亚甲基质子的立体专一性归属以及φ、ψ和χ1扭转角的范围。使用混合距离几何-动力学模拟退火方法以迭代方式进行结构计算。这涉及从实验数据的子集中计算一系列初始结构,以解决由于化学位移简并导致的一些NOE交叉峰归属中的模糊性。此外,这使我们能够利用从初始结构计算中获得的关于φ扭转角的信息,将立体专一性归属扩展到甘氨酸的α-亚甲基质子。最终的实验数据集包括554个质子间距离约束、12个氢键的24个约束以及33个φ、24个ψ和25个χ1扭转角约束。CT-CBH I有两个二硫键,其配对情况以前未知。对所有三种可能的二硫键组合以及无二硫键情况下计算的结构进行分析表明,正确的二硫键配对是8-25和19-35。用8-25和19-35二硫键计算了41个结构,各个结构与通过平均其坐标得到的平均结构之间的平均原子均方根偏差,主链原子为0.33±0.04 Å,所有原子为0.52±0.06 Å。该蛋白质呈楔形,具有两亲性,一面主要是亲水的,另一面主要是疏水的。二级结构的主要元件由一个不规则的三链反平行β-折叠组成,由残基5-9(β1)、24-28(β2)和33-36(β3)组成,其中β3链与其他两条链形成氢键。(摘要截短至400字)

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