This proposal will continue studies on the solution structures of? biologically active and potentially biomedically useful RNA enzymes? (ribozymes). There has been a major breakthrough in this work during the? previous grant period which was the development of methods for? isotopically labeling RNAs and subsequent application of the powerful? techniques of multi-dimensional heteronuclear magnetic resonance to the? solution structure determination of RNAs. The ribozymes that will be? studied include: i) a hammerhead ribozyme; ii) a hairpin ribozyme; and? iii) a lead-dependent self-cleaving ribozyme termed the leadzyme. These? ribozymes can all perform site-specific cleavage of a substrate RNA with? multiple turnover. The RNAs will be 13C/15N labeled and then a variety of? multi-dimensional heteronuclear magnetic resonance experiments will be? used to assign the proton, carbon and nitrogen resonances in these? molecules. Once resonance assignments have been made 2D, 3D, or 4D? heteronuclear NOESY-type experiments will be performed to obtain proton-? proton internuclear distances. Dihedral angle constraints will also be? obtained from other multi-dimensional NMR experiments. This distance and? dihedral angle information will be used as input for a distance geometry? algorithm or constrained molecular dynamics calculations to generate? three-dimensional structures consistent with the NMR data. The hammerhead? and hairpin ribozymes have site-specific RNA endonuclease activity and? have been shown to efficiently cleave specific sites in target RNAs in? vitro. There have also been several in vivo applications of these? ribozymes as RNA cleavage reagents against specific mRNAs, or as potential? antiviral agents that target the genome of an RNA virus such as HIV-l. The? structural information obtained from the NMR experiments proposed here? will provide valuable data for the design of improved ribozymes and will? be extremely helpful in interpretation of the wealth of biochemical,? kinetic and mutagenesis data on these ribozyme systems.?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37AI030726-17
Application #
7214173
Study Section
Special Emphasis Panel (NSS)
Program Officer
Tseng, Christopher K
Project Start
1990-12-01
Project End
2009-03-31
Budget Start
2007-04-01
Budget End
2008-03-31
Support Year
17
Fiscal Year
2007
Total Cost
$313,771
Indirect Cost
Name
University of Colorado at Boulder
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
007431505
City
Boulder
State
CO
Country
United States
Zip Code
80309
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Canny, Marella D; Jucker, Fiona M; Pardi, Arthur (2007) Efficient ligation of the Schistosoma hammerhead ribozyme. Biochemistry 46:3826-34
Lee, Joon-Hwa; Pardi, Arthur (2007) Thermodynamics and kinetics for base-pair opening in the P1 duplex of the Tetrahymena group I ribozyme. Nucleic Acids Res 35:2965-74
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Canny, Marella D; Jucker, Fiona M; Kellogg, Elizabeth et al. (2004) Fast cleavage kinetics of a natural hammerhead ribozyme. J Am Chem Soc 126:10848-9
Jucker, Fiona M; Phillips, Rebecca M; McCallum, Scott A et al. (2003) Role of a heterogeneous free state in the formation of a specific RNA-theophylline complex. Biochemistry 42:2560-7
Bondensgaard, Kent; Mollova, Emilia T; Pardi, Arthur (2002) The global conformation of the hammerhead ribozyme determined using residual dipolar couplings. Biochemistry 41:11532-42
Sibille, N; Pardi, A; Simorre, J P et al. (2001) Refinement of local and long-range structural order in theophylline-binding RNA using (13)C-(1)H residual dipolar couplings and restrained molecular dynamics. J Am Chem Soc 123:12135-46
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Hansen, M R; Simorre, J P; Hanson, P et al. (1999) Identification and characterization of a novel high affinity metal-binding site in the hammerhead ribozyme. RNA 5:1099-104

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