Understanding the factors controlling the photo-oxidation of natural DNA by enantiomerically pure intercalating ruthenium polypyridyl complexes through TA/TRIR studies with polydeoxynucleotides and mixed sequence oligodeoxynucleotides. Issue 32 (6th August 2020)

• Record Type: Journal Article
• Authors: Keane, Páraic M.; O'Sullivan, Kyra; Poynton, Fergus E.; Poulsen, Bjørn C.; Sazanovich, Igor V.; Towrie, Michael; Cardin, Christine J.; Sun, Xue-Zhong; George, Michael W.; Gunnlaugsson, Thorfinnur; Quinn, Susan J.; Kelly, John M.
• Is Part Of: Chemical science. Volume 11:Issue 32(2020)
• Page Start: 8600
• Page End: 8609
• Publication Date: 2020-08-06
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0sc02413a
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : Efficient electron transfer requires the complex to be intercalated at a G-C base-pair. Identification of preferred intercalation sites is achieved by TRIR monitoring of the nucleobase vibrations before electron transfer. Abstract : Ruthenium polypyridyl complexes which can sensitise the photo-oxidation of nucleic acids and other biological molecules show potential for photo-therapeutic applications. In this article a combination of transient visible absorption (TrA) and time-resolved infra-red (TRIR) spectroscopy are used to compare the photo-oxidation of guanine by the enantiomers of [Ru(TAP)2 (dppz)] 2+ in both polymeric {poly(dG-dC), poly(dA-dT) and natural DNA} and small mixed-sequence duplex-forming oligodeoxynucleotides. The products of electron transfer are readily monitored by the appearance of a characteristic TRIR band centred at ca. 1700 cm −1 for the guanine radical cation and a band centered at ca. 515 nm in the TrA for the reduced ruthenium complex. It is found that efficient electron transfer requires that the complex be intercalated at a G-C base-pair containing site. Significantly, changes in the nucleobase vibrations of the TRIR spectra induced by the bound excited state before electron transfer takes place are used to identify preferred intercalation sites in mixed-sequence oligodeoxynucleotides and natural DNA. Interestingly, with natural DNA, while it is found that quenching is inefficient in the picosecond range, a slower electron transfer process occurs, which is not found with the mixed-sequence duplex-forming oligodeoxynucleotides studied.