RNA-protein interactions are of paramount importance for gene regulation of viruses that cause human disease. The long term goal of this project is to understand the structural basis for the interaction of novel zinc finger proteins with the HIV-1 Rev responsive element (RRE) RNA, the binding site for the critical regulatory protein Rev. This knowledge will be exploited for developing small RRE binding proteins that possess both affinity and specificity in living cells. Using a powerful phage display approach that permits the sampling and scoring of a large number of proteins simultaneously, zinc finger proteins have been isolated which bind specifically to HIV-1 RRE and stem loop IIB. NMR structure determination is used to elucidate the zinc finger structure and specifics of RNA interaction. To enhance and further understand the RNA binding properties of zinc fingers, a design process will use structural information to guide in vitro selection as well as traditional site directed mutagenesis experiments. The molecular details of the interaction between zinc finger proteins and RRE stem loop IIB will be determined by NMR. The immediate goals of the proposal are three fold. First, to understand how these engineered proteins bind their RNA substrates by identifying binding sites and the amino acids responsible for RNA contact. Second, to improve their substrate affinity, Dr. Germann uses NMR structural data for site directed mutagenesis experiments and structure guided phage display selection. Finally, the limits and applicability of zinc fingers as inhibitors of biological processes will be determined by selection of zinc finger proteins against new RNA targets. The inhibitory activity of designed zinc fingers will be determined through in vitro and in vivo assays.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
7R01AI047459-02
Application #
6557985
Study Section
Molecular and Cellular Biophysics Study Section (BBCA)
Program Officer
Bridges, Sandra H
Project Start
2001-01-01
Project End
2005-12-31
Budget Start
2001-12-01
Budget End
2001-12-31
Support Year
2
Fiscal Year
2001
Total Cost
$117,791
Indirect Cost
Name
Georgia State University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
837322494
City
Atlanta
State
GA
Country
United States
Zip Code
30302
Thompson, R Adam; Spring, Alexander M; Sheng, Jia et al. (2015) The importance of fitting in: conformational preference of selenium 2' modifications in nucleosides and helical structures. J Biomol Struct Dyn 33:289-97
Johnson, Christopher N; Spring, Alexander M; Desai, Sunil et al. (2012) DNA sequence context conceals ?-anomeric lesions. J Mol Biol 416:425-37
Germann, Markus W; Johnson, Christopher N; Spring, Alexander M (2012) Recognition of damaged DNA: structure and dynamic markers. Med Res Rev 32:659-83
Johnson, Christopher N; Spring, Alexander M; Sergueev, Dimitri et al. (2011) Structural basis of the RNase H1 activity on stereo regular borano phosphonate DNA/RNA hybrids. Biochemistry 50:3903-12
Zhang, Jin; Germann, Markus W (2011) Characterization of secondary amide peptide bond isomerization: thermodynamics and kinetics from 2D NMR spectroscopy. Biopolymers 95:755-62
Khan, Ahmed M; Mishra, Subrata H; Germann, Markus W (2009) Cyclic enzymatic solid phase synthesis of isotopically labeled DNA oligonucleotides. Nucleosides Nucleotides Nucleic Acids 28:1030-41
Mishra, Subrata H; Spring, Alexander M; Germann, Markus W (2009) Thermodynamic profiling of HIV RREIIB RNA-zinc finger interactions. J Mol Biol 393:369-82
Zhang, Xinjian; Dou, Jun; Germann, Markus W (2009) Characterization of the cellular immune response in hepatitis C virus infection. Med Res Rev 29:843-66
Zhang, Jin; Spring, Alexander; Germann, Markus W (2009) Facilitated assignment of adenine H2 resonances in oligonucleotides using homonuclear long-range couplings. J Am Chem Soc 131:5380-1
Mazurek, Anthony; Johnson, Christopher N; Germann, Markus W et al. (2009) Sequence context effect for hMSH2-hMSH6 mismatch-dependent activation. Proc Natl Acad Sci U S A 106:4177-82

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