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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

Keane, P�raic M.; O'Sullivan, Kyra; Poynton, Fergus E.; Poulsen, Bj�rn C.; Sazanovich, Igor V.; Towrie, Michael; Cardin, Christine J.; Sun, Xue-Zhong; George, Michael W.; Gunnlaugsson, Thorfinnur; Quinn, Susan J.; Kelly, John M.

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 Thumbnail


Authors

P�raic M. Keane

Kyra O'Sullivan

Fergus E. Poynton

Bj�rn C. Poulsen

Igor V. Sazanovich

Michael Towrie

Christine J. Cardin

Thorfinnur Gunnlaugsson

Susan J. Quinn

John M. Kelly



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.

Citation

Keane, P. M., O'Sullivan, K., Poynton, F. E., Poulsen, B. C., Sazanovich, I. V., Towrie, M., …Kelly, J. M. (2020). 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. Chemical Science, 32, 8600-8609. https://doi.org/10.1039/d0sc02413a

Journal Article Type Article
Acceptance Date Jul 25, 2020
Online Publication Date Aug 6, 2020
Publication Date Aug 6, 2020
Deposit Date Sep 9, 2020
Publicly Available Date Sep 9, 2020
Journal Chemical Science
Print ISSN 2041-6520
Electronic ISSN 2041-6539
Publisher Royal Society of Chemistry
Peer Reviewed Peer Reviewed
Volume 32
Pages 8600-8609
DOI https://doi.org/10.1039/d0sc02413a
Keywords General Chemistry
Public URL https://nottingham-repository.worktribe.com/output/4816499
Publisher URL https://pubs.rsc.org/en/content/articlelanding/2020/sc/d0sc02413a

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