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Caught in the Loop: Binding of the [Ru(phen)2 (dppz)]2+ Light-Switch Compound to Quadruplex DNA in Solution Informed by Time-Resolved Infrared Spectroscopy.
Devereux, Stephen J; Poynton, Fergus E; Baptista, Frederico R; Gunnlaugsson, Thorfinnur; Cardin, Christine J; Sazanovich, Igor V; Towrie, Michael; Kelly, John M; Quinn, Susan J.
Affiliation
  • Devereux SJ; School of Chemistry, University College Dublin, Dublin, 4, Ireland.
  • Poynton FE; School of Chemistry, Trinity College Dublin, Dublin, 2, Ireland.
  • Baptista FR; Trinity Biomedical Sciences Institute (TBSI), Trinity College Dublin, Dublin, 2, Ireland.
  • Gunnlaugsson T; School of Chemistry, University College Dublin, Dublin, 4, Ireland.
  • Cardin CJ; School of Chemistry, Trinity College Dublin, Dublin, 2, Ireland.
  • Sazanovich IV; Trinity Biomedical Sciences Institute (TBSI), Trinity College Dublin, Dublin, 2, Ireland.
  • Towrie M; Department of Chemistry, University of Reading, Whiteknights, Reading, RG6 6AD, UK.
  • Kelly JM; Rutherford Appleton Laboratory, STFC, Harwell Campus, OX11 0FA, UK.
  • Quinn SJ; Rutherford Appleton Laboratory, STFC, Harwell Campus, OX11 0FA, UK.
Chemistry ; 26(71): 17103-17109, 2020 Dec 18.
Article in En | MEDLINE | ID: mdl-32725823
ABSTRACT
Ultrafast time-resolved infrared (TRIR) is used to report on the binding site of the [Ru(phen)2 (dppz)]2+ "light-switch" complex with both bimolecular (Oxytricha nova telomere) and intramolecular (human telomere) guanine-quadruplex structures in both K+ and Na+ containing solutions. TRIR permits the simultaneous monitoring both of the "dark" and "bright" states of the complex and of the quadruplex nucleobase bases, the latter via a Stark effect induced by the excited state of the complex. These data are used to establish the contribution of guanine base stacking and loop interactions to the binding site of this biologically relevant DNA structure in solution. A particularly striking observation is the strong thymine signal observed for the Na+ form of the human telomere sequence, which is expected to be in the anti-parallel conformation.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2020 Document type: Article Affiliation country: