Electronic Structure and Reactions of Fe-oxo Enzymes

Fe-oxo酶的电子结构和反应

• 批准号: 7088823
• 负责人: Louis Noodleman
• 金额: $ 22.91万
• 依托单位: SCRIPPS RESEARCH INSTITUTE, THE
• 依托单位国家: 美国
• 财政年份: 1991
• 资助国家: 美国
• 起止时间: 1991-05-01 至 2007-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7088823
• 关键词: Mossbauer spectrometry; active sites; circular magnetic dichroism; electron density; electron nuclear double resonance spectroscopy; enzyme activity; enzyme complex; enzyme structure; hemerythrin; iron; methane monooxygenase; quantum chemistry; ribonucleotide reductase

DESCRIPTION (provided by applicant): Theoretical calculations of the electronic structure of iron-oxo dimer complexes relevant to biology are now making important contributions to bioinorganic chemistry. High-accuracy density functional theory (DFT) methods are used to describe the transition metal dimer complex active site. The active site complex is then embedded in the longer range protein and solvent environment using an electrostatics and dielectric based representation for the evaluation of energetic interactions. The long-term goal is to develop a detailed understanding of critical intermediates, enzymatic mechanisms, reaction pathways, and energetics in iron-oxo dimer enzymes. These features will be related to the underlying electronic and geometric structure of the active site as a function of oxidation state, ligand environment and the protein surroundings. The iron-oxo enzymes to be studied are methane monooxygenase (MMO) and ribonucleotide reductase (RNR), which hydroxylate alkanes and reduce ribonucleotides (NDP) to deoxyribonucleotides (dNDP), respectively. The major goals of the project include: (1) Using DFT methods to calculate optimal active site geometries with associated energies for a number of feasible structures of key intermediates in MMO and RNR, which will then be compared with experimental structural results from spectroscopies or X-ray structures; (2) To evaluate reaction pathways and comparative energetics of different enzymes and mutants; (3) To make important connections with experimental data by comparing calculated spectroscopic properties from DFT electronic structures with corresponding experimental results from optical, MCD, Mossbauer and ENDOR spectroscopies, and from magnetic susceptibility measurements. These comparisons are very important for those critical intermediates of the catalytic cycles where X-ray structures are not available, particularly intermediate Q of MMO and intermediate X of RNR; (4) To extend and improve the current quantum mechanics/electrostatics methodology to full quantum mechanics/molecular mechanics (QM/MM) with multiple dielectric regions for the quantum cluster, protein and solvent.

描述（由申请人提供）：与生物学相关的铁-氧代二聚体复合物的电子结构的理论计算现在对生物无机化学做出了重要贡献。 采用高精度密度泛函理论（DFT）方法对过渡金属二聚体配合物的活性中心进行了研究。 活性位点复合物，然后嵌入在较长的范围内的蛋白质和溶剂环境中使用的静电和介电为基础的代表性的评价充满活力的相互作用。 长期的目标是发展一个详细的了解关键中间体，酶的机制，反应途径，并在铁氧二聚体酶的能量学。 这些功能将涉及到潜在的电子和几何结构的活性位点的氧化态，配体环境和蛋白质周围的功能。 要研究的铁氧化酶是甲烷单加氧酶（MMO）和核糖核苷酸还原酶（RNR），它们分别将烷烃羟基化和将核糖核苷酸（NDP）还原为脱氧核糖核苷酸（dNDP）。 本项目的主要目标包括：（1）利用DFT方法计算MMO和RNR关键中间体的最佳活性中心几何构型和相关能量，并与光谱或X射线结构的实验结果进行比较;（2）评估不同酶和突变体的反应途径和比较能量学;（3）将DFT电子结构计算的光谱性质与光学、MCD、Mossbauer和ENDOR光谱以及磁化率测量的相应实验结果进行比较，与实验数据建立重要联系。这些比较对于那些没有X射线结构的催化循环的关键中间体是非常重要的，特别是MMO的中间体Q和RNR的中间体X;（4）将现有的量子力学/静电学方法扩展和改进到量子簇、蛋白质和溶剂的具有多个介电区域的全量子力学/分子力学（QM/MM）。