Biomolecular Interactions and Enzymatic Processes

生物分子相互作用和酶促过程

• 批准号: 8538402
• 负责人: JIALI GAO
• 金额: $ 28.86万
• 依托单位: UNIVERSITY OF MINNESOTA
• 依托单位国家: 美国
• 财政年份: 1992
• 资助国家: 美国
• 起止时间: 1992-09-30 至 2016-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8538402
• 关键词: Address; Amino Acids; Area; Binding; Biochemical Process; Biochemical Reaction; Biological; Biological Process; Catalysis; Cells; Charge; Chemicals; Chemistry; Coenzymes; Comparative Study; Complex; Computer Simulation; Computing Methodologies; Coupled; Data; Development; Disease; Electron Transport; Electronics; Electrons; Engineering; Enzymes; Epigenetic Process; Evaluation; Excision; Flavin-Adenine Dinucleotide; Free Energy; Free Radicals; Goals; Grant; Growth; Heme; Histones; Hydrogen; Iron; Kinetics; Knowledge; Life; Lysine; Malignant Neoplasms; Masks; Mechanics; Metabolism; Methodology; Methods; Microscopic; Modeling; Molecular; Nuclear; Oxygen; Pharmaceutical Preparations; Pharmacologic Substance; Photosynthesis; Play; Principal Investigator; Procedures; Process; Property; Protein Dynamics; Protein Engineering; Proteins; Protons; Reaction; Regulation; Research; Research Project Grants; Resolution; Respiration; Ribonucleotide Reductase; Role; Solutions; Structure; Techniques; Testing; Theoretical model; Translations; Veins; Water; aqueous; arginyllysine; biological systems; cell growth; chemical reaction; cofactor; computer studies; demethylation; density; design; enzyme mechanism; histone modification; improved; inhibitor/antagonist; insight; interest; methyl group; molecular dynamics; molecular orbital; oxidation; programs; quantum; research study; simulation; structural biology; theories; tool

DESCRIPTION (provided by applicant): A multi-faceted research project is directed aimed at computational studies of enzymatic processes in aqueous solution. The theoretical approach centers on molecular dynamics free energy simulations of enzymes, making use of combined quantum mechanical and molecular mechanical (QM/MM) methods. A major goal is to increase the capability of QM/MM methods and to achieve greater accuracy than conventional approaches. We propose to further improve the mixed molecular orbital and valence bond (MOVB) theory, coupled with the self-consistent charge tight-bonding density functional theory (SCC-DFTB) and extension to the CHARMM program with ab initio and DFT methods, such that the theoretical model can be conveniently calibrated, tested and used by experimental biochemists as a research tool to help interpret experiment findings. The MOVB method has been developed at theoretical levels that include ab initio and semiempirical molecular orbital and density functional theory. One goal of the present study is to incorporate the procedure into molecular dynamics simulation programs for effectively modeling enzymatic reactions. A major thrust of this project is to provide a deeper understanding of the underlying principles and mechanisms of enzymatic reactions. During this grant period, we focus on the catalytic mechanism of histone lysine demethylases with emphasis on the Jumonji C domain containing enzymes, which belong to a large class of enzymes that utilize a non-heme high- valent iron-oxo intermediate. Histone lysine demethylases along with other histone protein modifying enzymes play a critical role in epigenetic regulation and have been found to be associated with cancer development and progress. In addition, we seek to address the general properties of enzymatic proton-coupled electron transfer reactions and the effects of protein dynamics and enzyme reorganization energies on these processes. The MOVB method provides an important research tool to study these questions, and the results will be of general importance to protein engineering and inhibitor design. PHS 398/2590 (Rev. 06/09) Page Continuation Format Page

描述（由申请人提供）：一个多方面的研究项目旨在对水溶液中的酶过程进行计算研究。理论方法集中在酶的分子动力学自由能模拟，利用结合量子力学和分子力学（QM/MM）方法。一个主要的目标是提高能力的QM/MM方法，并实现更高的精度比传统的方法。我们建议进一步改进混合分子轨道和价键（MOVB）理论，结合自洽电荷紧键密度泛函理论（SCC-DFTB），并利用从头算和密度泛函方法对CHARMM程序进行扩展，使理论模型可以方便地被实验生物化学家校准、检验和使用，作为解释实验结果的研究工具。MOVB方法已经发展到理论水平，包括从头算和半经验分子轨道和密度泛函理论。本研究的一个目标是将该程序纳入分子动力学模拟程序，以有效地模拟酶促反应。该项目的一个主要目标是更深入地了解酶反应的基本原理和机制。在此期间，我们专注于组蛋白赖氨酸脱甲基酶的催化机制，重点是含Jumonji C结构域的酶，其属于利用非血红素高价铁-氧代中间体的一大类酶。组蛋白赖氨酸脱甲基酶沿着其他组蛋白修饰酶在表观遗传调控中起关键作用，并且已发现与癌症的发展和进展相关。此外，我们试图解决酶的质子耦合电子转移反应的一般性质和蛋白质动力学和酶重组能量对这些过程的影响。MOVB方法为研究这些问题提供了一个重要的研究工具，其结果对蛋白质工程和抑制剂设计具有重要意义。PHS 398/2590（Rev.06/09）