This proposal is the second five-year competitive renewal request to continue our ongoing program project studies of DNA structure, dynamics and recognition for the period 1994-98. The solution structure of a variety of biologically important sequences (synthesized in the Core lab) will be studied by chemical probe methods and by high-resolution NRM distance geometry methods. In parallel studies the sequence-dependent dynamics of DNA will be investigated on various timescales via a variety f spectroscopic relaxation techniques, including solid-state NMR, solution-state NMR, EPR (pulsed ELDOR and CW methods) and laser optical (FPA & DLS) methods. Structural measurements using isotopically labelled DNA (synthesized by the Core lab) will also be carried out using solid-state methods (REDOR/DRAMA). The structure of zinc-finger proteins that recognize specific DNA sequences will be determined by high-resolution NMR. Finally, the Core lab will supervise and coordinate the construction of a new 750 MHz NMR spectrometer to increase the sensitivity and resolution of ongoing NMR studies, as well as continuing its role as a DNA synthesis facility by providing normal and isotopically labelled nucleic acid sequences to the participating research groups.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Program Projects (P01)
Project #
5P01GM032681-14
Application #
2021975
Study Section
Special Emphasis Panel (ZRG7-SSS-7 (04))
Project Start
1984-01-01
Project End
1998-12-31
Budget Start
1997-01-01
Budget End
1997-12-31
Support Year
14
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Washington
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
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Geahigan, K B; Meints, G A; Hatcher, M E et al. (2000) The dynamic impact of CpG methylation in DNA. Biochemistry 39:4939-46

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