In the environment DNA is subject to damage by a wide variety of chemical and physical agents. In particular, ultraviolet (UV) light can cause photochemical [2+2] cycloadditions of pyrimidine bases which are adjacent and on the same strand. The survival of any organism depends on its ability to locate and repair any DNA lesions such as pyrimidine dimers, before the error is propogated. Several DNA repair pathways exist in nature. The subject of this study is the so-called """"""""light"""""""" repair pathway in which pyrimidine dimers are monomerized by a class of enzymes called photolyases. Photolyases are activated by light.
The aim of this project is to understand the photochemical process that is utilized by photolyase to repair DNA. To accomplish this we will use the tools of mechanistic photochemistry such as time-resolved laser spectroscopy, fluorescence quenching, synthesis of model substrates and EPR spectroscopy. The investigation will begin with simple, well-defined model systems and use the knowledge gained there to interpret the data from the more relevant (and complicated) enzymic system.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29GM045856-03
Application #
2183455
Study Section
Molecular and Cellular Biophysics Study Section (BBCA)
Project Start
1992-02-01
Project End
1997-01-31
Budget Start
1994-02-01
Budget End
1995-01-31
Support Year
3
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Maryland College Park
Department
Chemistry
Type
Schools of Earth Sciences/Natur
DUNS #
City
College Park
State
MD
Country
United States
Zip Code
20742