ACETOPHENONE PHOTOSENSITIZATION OF THYMINE DIMER FORMATION IN AQUEOUS-SOLUTIONS OF CALF THYMUS DNA

Citation
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
Citations number
19
Categorie Soggetti
Chemistry
ISSN journal
03794350
Volume
47
Issue
2
Year of publication
1994
Pages
48 - 52
Database
ISI
SICI code
0379-4350(1994)47:2<48:APOTDF>2.0.ZU;2-Y
Abstract
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.