| Literature DB >> 26587711 |
James P Hall1,2, Fergus E Poynton3,4, Páraic M Keane1,3, Sarah P Gurung1,2, John A Brazier5, David J Cardin1, Graeme Winter2, Thorfinnur Gunnlaugsson3,4, Igor V Sazanovich6, Michael Towrie6, Christine J Cardin1, John M Kelly3, Susan J Quinn7.
Abstract
To understand the molecular origins of diseases caused by ultraviolet and visible light, and also to develop photodynamic therapy, it is important to resolve the mechanism of photoinduced DNA damage. Damage to DNA bound to a photosensitizer molecule frequently proceeds by one-electron photo-oxidation of guanine, but the precise dynamics of this process are sensitive to the location and the orientation of the photosensitizer, which are very difficult to define in solution. To overcome this, ultrafast time-resolved infrared (TRIR) spectroscopy was performed on photoexcited ruthenium polypyridyl-DNA crystals, the atomic structure of which was determined by X-ray crystallography. By combining the X-ray and TRIR data we are able to define both the geometry of the reaction site and the rates of individual steps in a reversible photoinduced electron-transfer process. This allows us to propose an individual guanine as the reaction site and, intriguingly, reveals that the dynamics in the crystal state are quite similar to those observed in the solvent medium.Entities:
Mesh：
Substances：
Year: 2015 PMID： 26587711 DOI： 10.1038/nchem.2369
Source DB: PubMed Journal: Nat Chem ISSN： 1755-4330 Impact factor: 24.427