OXIDATION OF DNA AND RNA BY OXORUTHENIUM(IV) METALLOINTERCALATORS - VISUALIZING THE RECOGNITION PROPERTIES OF DIPYRIDOPHENAZINE BY HIGH-RESOLUTION ELECTROPHORESIS

Citation
Pj. Carter et al., OXIDATION OF DNA AND RNA BY OXORUTHENIUM(IV) METALLOINTERCALATORS - VISUALIZING THE RECOGNITION PROPERTIES OF DIPYRIDOPHENAZINE BY HIGH-RESOLUTION ELECTROPHORESIS, Journal of the American Chemical Society, 120(4), 1998, pp. 632-642
Citations number
80
Categorie Soggetti
Chemistry
ISSN journal
00027863
Volume
120
Issue
4
Year of publication
1998
Pages
632 - 642
Database
ISI
SICI code
0002-7863(1998)120:4<632:OODARB>2.0.ZU;2-4
Abstract
The binding specificity for the intercalating Ru(tpy)(dppz)O2+ complex (tpy = 2,2',2 ''-terpyridine; dppz = dipyridophenazine) was investiga ted fur duplex DNA, HN-I TAR DNA and RNA? and tRNA(Phe) Unlike other d ppz compounds studied to date, this compound cleaves nucleic acids at short range, and the resulting cleavage pattern dan therefore be direc tly related to the recognition properties of the dppz ligand. To assig n the intercalative recognition sites, a comparison was first made bet ween the cleavage patterns of Ru(tpy)(dppz)O2+ and Hu(tpy)(bpy)O2+ (bp y = 2,2'-bipyridine), which differs from Ru(tpy)(dppz)O2+ only by the absence of the intercalative dppz functionality. Cleavage sites common to both complexes were assigned to binding properties other than inte rcalation, whereas any additional sites observed for Ru(tpy)(dppz)O2were strongly implicated as the sites of intercalative recognition. It was necessary, however, to distinguish between those sites which repr esent a strong binding affinity and those sites which were instead mad e more accessible to cleavage by binding of another equivalent of the Intercalating complex at a remote site. We therefore investigated the cleavage pattern of Ru(tpy)(bpy)O2+ with and without the classical int ercalator Pt(tpy)(HET)(+) (HET = 2-hydroxyethanethiolate) to determine the effect of decoupling the intercalative recognition and oxidation chemistry, In this experiment, sites where cleavage inhibition was obs erved were indicative of intercalative recognition by the platinum com plex, whereas sites where cleavage enhancement was observed strongly s uggested that intercalative binding at a remote site had altered the s tructure of the nucleic acid. Comparison of the cleavage patterns of R u(tpy)(bpy)O2+ and Ru(tpy)(dppz)O2+ for a duplex oligonucleotides. tRN A, and stem-loop structures suggests a recognition pattern for the dpp z ligand very similar to that pf classical intercalators.