Hairpin Ribozyme: Folding, Structure and Mechanism

发夹核酶：折叠、结构和机制

• 批准号: 6869828
• 负责人: JOHN MacKenzie BURKE
• 金额: $ 48.78万
• 依托单位: UNIVERSITY OF VERMONT & ST AGRIC COLLEGE
• 依托单位国家: 美国
• 财政年份: 1998
• 资助国家: 美国
• 起止时间: 1998-12-01 至 2009-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6869828
• 关键词: active sites; crosslink; enzyme mechanism; enzyme substrate complex; fluorescence spectrometry; functional /structural genomics; gene mutation; molecular dynamics; nucleic acid structure; protein folding; ribosomes; ribozymes; spliceosomes

DESCRIPTION (provided by applicant) An integrated series of biochemical, biophysical, combinatorial, and molecular simulation experiments is presented, designed to address three fundamental questions concerning the hairpin ribozyme. First, how does the RNA fold into its native structure? Second, what are the key features of active site architecture? Third, what is the catalytic mechanism? Recent advances make it possible to answer these questions during the next funding period. These advances include: (a) development of methods to analyze folding events at the molecular and nucleobase levels, (b) demonstration that a combination of bench biochemistry and computational methods can lead to the modeling and experimental verification of specific tertiary interactions at the active site, (c) elucidation of crystal structures of the ribozyme, (d) discovery that G8 participates in metal-independent active site chemistry, and (e) the ability to execute a sophisticated 'genetic' analysis through in vitro selection. Specific Aims are: (1) Identify the structural and functional roles of specific nucleotides and functional groups implicated in catalysis and folding; (2) Isolate peudorrevertants of inactivating mutations by in vitro selection, and establish the mechanism of functional compensation; (3) Characterize and model conformational changes during the catalytic cycle, and determine which are necessary for catalytic function; (4) Develop and test models of the catalytic mechanism. The biomedical importance of this work includes (i) the advancement of our understanding of RNA structure and how it leads to catalytic activity, (ii) understanding biological reactions catalyzed by ribozymes and ribonucleoprotein complexes (including the ribosome and the spliceosome) in biological reactions, and (iii) the application of our understanding of catalytic RNA and ribozyme engineering to improving health, through functional genomics, pharmaceutical target validation, and the development of selective ribozyme based therapeutics for genetic and viral diseases.

描述(由申请人提供)提出了一系列综合的生化、生物物理、组合和分子模拟实验，旨在解决有关发夹核酶的三个基本问题。首先，RNA是如何折叠成其天然结构的？第二，Active Site架构的主要特征是什么？第三，催化机制是什么？最近取得的进展使我们有可能在下一个供资期间回答这些问题。这些进展包括：(A)在分子和碱基水平上分析折叠事件的方法的发展；(B)证明台式生物化学和计算方法的结合可以导致对活性位点上特定的三级相互作用的建模和实验验证；(C)核酶的晶体结构的阐明；(D)发现G8参与不依赖于金属的活性位点化学；以及(E)通过体外选择执行复杂的‘遗传’分析的能力。具体目标是：(1)确定催化和折叠过程中涉及的特定核苷酸和官能团的结构和功能作用；(2)通过体外选择分离失活突变的伪可逆株，并建立功能补偿机制；(3)表征和模拟催化循环中的构象变化，并确定哪些是催化功能所必需的；(4)开发和测试催化机制的模型。这项工作的生物医学重要性包括：(I)促进我们对RNA结构及其如何导致催化活性的理解，(Ii)了解核酶和核糖核蛋白复合体(包括核糖体和剪接体)在生物反应中催化的生物反应，以及(Iii)通过功能基因组学、药物靶点验证以及开发基于核酶的选择性核酶治疗遗传和病毒疾病的方法，将我们对催化RNA和核酶工程的理解应用于改善健康。