CONFORMATIONAL STUDIES OF THE (-TRANS-ADDUCTS, (-)-TRANS-ADDUCTS, (+)-CIS-ADDUCTS, AND (-)-CIS-ADDUCTS OF ANTI-BENZO[A]PYRENE DIOLEPOXIDE TO N-2-DG IN DUPLEX OLIGONUCLEOTIDES USING POLYACRYLAMIDE-GEL ELECTROPHORESIS AND LOW-TEMPERATURE FLUORESCENCE SPECTROSCOPY())

Using polyacrylamide gel electrophoresis (PAGE) and low-temperature, l aser-induced fluorescence line narrowing (FLN) and non-line narrowing (NLN) spectroscopic methods, the conformational characteristics of ste reochemically defined and site-specific adducts derived from the bindi ng of 7 beta,8 alpha-dihydroxy-9 alpha,10 alpha-epoxy-7,8,9,10-tetrahy drobenzo[a]pyrene (anti-BPDE, a metabolite of the environmental carcin ogen benzo[a]pyrene), to DNA were studied. The focus of these studies was on the four stereochemically distinct anti-BPDE modified duplexes 5'-d(CCATCGCTACC).(GGTAGCGATGG), where G denotes the lesion site deriv ed from trans or cis addition of the exocyclic amino group of guanine to the C10 position of either(+) or(-)-anti-BPDE. PAGE experiments und er non-denaturing conditions showed that the(+)-trans adduct causes a significantly greater retardation in the electrophoretic mobility than the other three adducts, probably the result of important adduct-indu ced distortions of the duplex structure, Low-temperature fluorescence studies in frozen aqueous buffer matrices showed that the(+)-trans add uct adopts primarily an external conformation with only minor interact ions with the helix, but a smaller fraction(similar to 25%) appears to exists in a partially base-stacked conformation. The(-)-trans adduct exists almost exclusively (similar to 97%) in an external conformation . Both cis adducts were found to be intercalated; strong electron-phon on coupling observed in their FLN spectra provided additional evidence for significant pi-pi stacking interactions between the pyrenyl resid ues and the bases. FLN spectroscopy is shown to be suitable for distin guishing between trans and cis adducts, but lesions with either(+)- or (-)-trans, or (+)- or (-)-cis stereochemical characteristics showed v ery similar vibrational patterns. Addition of glycerol (50%, v/v) to t he matrix caused a partial disruption of the chromophore-base stacking interactions for most adducts, but the (-)-cis isomer showed a strong blue-shift and unusual vibrational frequencies. Low-temperature fluor escence spectroscopy techniques are most suitable for distinguishing b etween different conformational benzo[a]pyrene diol epoxide-DNA adduct types; because of the sensitivity of these methods, they may provide important information necessary for an understanding of the biological effects of the stereochemically distinct BPDE-guanine lesions.