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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.
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DOI: 10.1021/bi992024s
发表时间: 1999
期刊: Biochemistry
影响因子: 2.9
作者: [Pinard,R, Lambert,D, Walter,NG, Heckman,JE, Major,F, Burke,JM]
通讯作者: Burke,JM
Modifications and deletions of helices within the hairpin ribozyme-substrate complex: an active ribozyme lacking helix 1.
发夹核酶-底物复合物内螺旋的修饰和缺失:缺乏螺旋 1 的活性核酶。
DOI: 10.1261/rna.5650904
发表时间: 2004
期刊: RNA (New York, N.Y.)
影响因子: --
作者: [Pinard,Robert, Lambert,Dominic, Pothiawala,Gulnar, Major,François, Burke,JohnM]
通讯作者: Burke,JohnM
A conformational change in the "loop E-like" motif of the hairpin ribozyme is coincidental with domain docking and is essential for catalysis.
发夹核酶的“环E样”基序的构象变化与结构域对接一致,并且对于催化是必需的。
DOI: 10.1021/bi0028385
发表时间: 2001
期刊: Biochemistry
影响因子: 2.9
作者: [Hampel,KJ, Burke,JM]
通讯作者: Burke,JM
Cobalt(III)hexaammine-dependent photocrosslinks in the hairpin ribozyme.
发夹核酶中钴(III)六氨依赖性光交联。
DOI: 10.1016/j.jinorgbio.2013.11.001
发表时间: 2014
期刊: Journal of inorganic biochemistry
影响因子: 3.9
作者: [Kraemer-Chant,ChristinaM, Heckman,JoyceE, Lambert,Dominic, Burke,JohnM]
通讯作者: Burke,JohnM
Enhancing Protections through Learner-Centered Education
Hammerhead Ribozyme: Active Site Assembly and Structure
Hammerhead Ribozyme: Active Site Assembly and Structure
Hammerhead Ribozyme: Active Site Assembly and Structure
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