NMR and EPR Studies of Ribozyme Catalytic Mechanisms

核酶催化机制的 NMR 和 EPR 研究

基本信息

批准号：
7931125
负责人：
CHARLES G HOOGSTRATEN
金额：
$ 7万
依托单位：
MICHIGAN STATE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-09-30 至 2010-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7931125
关键词：
Address Affect Binding Binding Sites Biochemical Energetics Biological Assay Catalysis Catalytic Domain Catalytic RNA Chemistry Complement Complex Coupled Coupling DNA Sequence Rearrangement Data Development Disease Docking Goals Heteronuclear NMR Ions Kinetics Label Left Ligation Link Magnetic Resonance Maps Messenger RNA Metal Ion Binding Metals Methods Molecular Molecular Conformation Molecular Structure Mutation Pathway interactions Physiologic pulse Play Positioning Attribute Process Property RNA RNA Splicing Reaction Relaxation Research Personnel Role Scheme Site Spliceosomes Structure Substrate Domain System Techniques Testing Therapeutic Thermodynamics U6 small nuclear RNA Ursidae Family Variant Work catalyst cofactor comparative design divalent metal fascinate hairpin ribozyme interest leadzyme mRNA Precursor new technology novel programs research study stem tool

项目摘要

DESCRIPTION (provided by applicant): The overarching goal of this project is to develop a detailed biophysical understanding of the mechanism of action of catalytic RNA molecules, or ribozymes. Ribozyme derivatives are currently under development as therapeutics for a number of devastating diseases. A fundamental understanding of ribozyme mechanism is critical in the design of derivatives, with necessary improvements in pharmacological properties that simultaneously maintain the desired catalytic activity. Our thesis, is that, the static structure of a ribozyme is insufficient to understand its mechanism of action, and that structural work must be coupled with studies of the molecule's dynamics, its interactions with multivalent metal ions, and the effects of those metal ions on molecular structure and dynamics. We will apply contemporary magnetic resonance techniques, including heteronuclear NMR spin relaxation and advanced EPR experiments, to provide unique information that bears directly on these issues and, thus, to link structural studies with biochemical energetics. The dynamic properties of ribozyme conformations, as studied by NMR spin relaxation, will be emphasized. In the well characterized hairpin ribozyme, we will investigate the dynamic properties of the molecule using NMR spin relaxation in active vs. inactive sequence variants, and as a function of tertiary structure formation (docking). We will proceed to use an integrated EPR and NMR approach, to delineate the effects of multivalent metal ions, which are crucial for catalysis, but do not participate directly in chemistry in this system, on the ribozyme's structure and dynamics. We are also interested in the U6 snRNA, a catalytically critical component of the eukaryotic mRNA splicing apparatus. In this system, we will investigate the structure of a biochemically-identified metal ion, which appears to participate in reaction chemistry, both in the internal stemloop that forms its immediate binding site, and in larger complexes, including pre-mRNA sequences. Studies of these two systems will provide complementary and synergistic perspectives on the interrelationships among conformational dynamics, metal ion cofactor ligation, and catalytic function in RNA. In short, we propose an integrated biophysical program of technological progress and novel applications, that will significantly advance the ribozyme field toward a molecular-level understanding of these fascinating catalysts.

描述（由申请人提供）：该项目的总体目标是对催化 RNA 分子或核酶的作用机制产生详细的生物物理学理解。目前正在开发核酶衍生物作为许多破坏性疾病的治疗方法。对核酶机制的基本了解对于衍生物的设计至关重要，需要改进药理学特性，同时保持所需的催化活性。我们的论文是，核酶的静态结构不足以理解其作用机制，结构工作必须与分子动力学、其与多价金属离子的相互作用以及这些金属离子对核酶的影响的研究相结合。分子结构和动力学。我们将应用当代磁共振技术，包括异核核磁共振自旋弛豫和先进的 EPR 实验，提供与这些问题直接相关的独特信息，从而将结构研究与生化能量学联系起来。将强调通过核磁共振自旋弛豫研究的核酶构象的动态特性。在充分表征的发夹核酶中，我们将使用活性与非活性序列变体中的 NMR 自旋弛豫以及作为三级结构形成（对接）的函数来研究分子的动态特性。我们将继续使用集成的 EPR 和 NMR 方法来描述多价金属离子对核酶结构和动力学的影响，多价金属离子对催化至关重要，但不直接参与该系统的化学反应。我们还对 U6 snRNA 感兴趣，它是真核 mRNA 剪接装置的催化关键组件。在这个系统中，我们将研究生化鉴定的金属离子的结构，该金属离子似乎参与反应化学，无论是在形成其直接结合位点的内部茎环中，还是在更大的复合物中，包括前mRNA序列。对这两个系统的研究将为构象动力学、金属离子辅因子连接和 RNA 催化功能之间的相互关系提供互补和协同的视角。简而言之，我们提出了一个技术进步和新颖应用的综合生物物理计划，这将显着推进核酶领域对这些迷人催化剂的分子水平理解。