"There's a lot of discussion in the literature about how damaged DNA is recognized by the repair enzymes," said Maciej Haranczyk, a staff scientist at the Department of Energy's Pacific Northwest National Laboratory in Richland, Wash. "The current picture is that some enzymes bend damaged DNA in order to repair altered fragments. But no one knew why damaged DNA was more susceptible to bending."

Haranczyk and colleagues' simulation, reported Sunday at the American Chemical Society national meeting, offers an explanation. First, they programmed a chemical change to an intact DNA fragment. As with real DNA, the simulated molecule's backbone became distorted and its base pairs displaced. The structural change corresponded with a change in the molecule's shape, in its energy and how electric charges are distributed throughout the molecule.

"All these features are significant in enzymatic recognition of the damaged site," Haranczyk said. "In our model, damage triggers a reorganization of the sugar-phosphate in the DNA's backbone such that the DNA becomes thinner. In damaged DNA, negatively charged phosphate groups migrate along the axis of the DNA, and that allows the molecule to bend easily. We believe it is this difference in the damaged and intact DNA that the enzymes recognize."

Haranczyk said this was the first quantum chemistry simulation to survey such a large biological system--in this case, a DNA fragment made up of 350 atoms. "With a system so big, one can't do this kind of work without a supercomputer. Fortunately, we had access to one of the world's 10 most powerful computers," housed at the W.R. Wiley Environmental Molecular Sciences Laboratory on the PNNL campus.

PNNL ( '"/>

Contact: Bill Cannon
cannon@pnl.gov
509-375-3732
DOE/Pacific Northwest National Laboratory
22-Aug-2004