Lf. Salter et R. Thomas, ACETOPHENONE PHOTOSENSITIZATION OF THYMINE DIMER FORMATION IN AQUEOUS-SOLUTIONS OF CALF THYMUS DNA, South African Journal of Chemistry, 47(2), 1994, pp. 48-52
The acetophenone-photosensitized formation of the cis-syn cyclobutane
thymine dimer between two contiguous thymines on a strand of naked cal
f thymus DNA has been used to construct a preliminary model for the re
action kinetics of DNA. Eleven elementary steps have been proposed to
describe the processes involved. Rate constants were initially assigne
d either from analogous values in the literature or by calculation for
reactions that were thought to be diffusion controlled. The reaction
scheme was then computer simulated and the rate constants were optimiz
ed to give agreement between the predictions of the computer model and
the experimental data. The values arrived at in this manner agreed wi
th those obtained from Stern-Volmer plots based on the mechanism. Mech
anisms of the type proposed here could be used to provide a quantitati
ve basis for the relationship between absorbed radiation and cellular
events, in particular those causing cell death. Similar mechanisms cou
ld be applied to the reactions of DNA with chemicals.