Redox Pathways in DNA Oxidation:  Kinetic Studies of Guanine and Sugar Oxidation by Para-Substituted Derivatives of Oxoruthenium(IV)

• Published in: Inorganic chemistry Vol. 39; no. 1; pp. 44 - 49
• Main Authors: Farrer, Brian T, Thorp, H. Holden
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 10.01.2000
• Subjects: Carbohydrates - chemistry; Deoxycytidine Monophosphate - chemistry; DNA - chemistry; Electrochemistry; Guanine - chemistry; Guanosine Monophosphate - chemistry; Kinetics; Organometallic Compounds - chemistry; Oxidation-Reduction; Ruthenium Compounds - chemistry; Spectrophotometry, Ultraviolet
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/ic990833u

The oxidation of nucleotides and DNA by a series of complexes based on Ru(tpy)(bpy)O2+ (1) was investigated (tpy = 2,2‘:6‘,2‘ ‘-terpyridine; bpy = 2,2‘-bipyridine). These complexes were substituted with electron-donating or -withdrawing substituents in the para positions of the polypyridyl ligands so that the oxidation potentials of the complexes were affected but the reaction trajectory of the oxo ligand with DNA was the same throughout the series. The prepared complexes were (with E 1/2(III/II) and E 1/2(IV/III) values in volts versus Ag/AgCl) Ru(4‘-EtO-tpy)(bpy)O2+ (2; 0.47, 0.60), Ru(4‘-Cl-tpy)(bpy)O2+ (3; 0.55, 0.63), Ru(tpy)(4,4‘-Me2-bpy)O2+ (4; 0.48, 0.62), and Ru(tpy)(4,4‘-Cl2-bpy)O2+ (5; 0.58, 0.63). The complexes oxidized deoxycytosine 5‘-monophosphate at the sugar moiety (k = 0.24−0.47 M-1 s-1) and guanosine 5‘-monophosphate at the base moiety (k = 6.1−15 M-1 s-1). The rate constants increase across these ranges in the order 3 > 1 > 4 > 2, which is the same order as the redox potentials of the complexes. The effect of the base on these reactions was also studied, and xanthine was found to react with 1 much faster than guanine while hypoxanthine was less reactive than the sugar moiety. The complexes all oxidized oligonucleotides to generate base-labile lesions at guanine and a combination of spontaneous and base-labile scission at the sugar functionalities. The selectivity of cleavage in duplex and single-stranded DNA was not a strong function of the substituents on the metal complex.