The interaction of calf-thymus DNA with aspirin is investigated in aqu
eous solution at pH 7-6 with drug/DNA(phosphate) molar ratios of r = 1
/40, 1/20, 1/10, 1/5, 1/2, 1 and 2. Fourier transform infrared (FTIR)
and laser Raman difference spectroscopy are used to determine drug bin
ding sites, sequence preference and DNA secondary structure, as well a
s the structural variations of aspirin-DNA complexes in aqueous soluti
on, Spectroscopic evidence showed that at low aspirin concentration (r
= 1/40), drug-DNA interaction is mainly through the backbone PO2 grou
ps and the A-T base pairs, Such interaction largely perturbs the phosp
hate vibration at 1222 cm(-1) and the A-T bands at 1663 and 1609 cm(-1
) with no major helix destabilization. At higher drug concentration (r
> 1/20), the participation of the G-C bases in drug-DNA complexation
was evident by strong perturbations of the guanine and cytosine vibrat
ions at 1717 and 1494 cm(-1), with a partial helix destabilization. A
major alteration of the B-DNA structure towards A-DNA occurs on drug c
omplexation, The aspirin interaction was through anion CO and COOCH3 d
onor atoms with those of the backbone PO2 group and DNA bases donor si
tes (directly or indirectly via H2O molecules).