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Photo‐oxidizing Ruthenium(II) Complexes with Enhanced Visible Light Absorption and G‐quadruplex DNA Binding Abilities

Authors :
UCL - SST/IMCN/MOST - Molecular Chemistry, Materials and Catalysis
Gillard, Martin
Piraux, Guillaume
Daenen, Martin
Abraham, Michael
Troian-Gautier, Ludovic
Bar, Laure
Bonnet, Hugues
Loiseau, Frédérique
Jamet, Hélène
Dejeu, Jérome
Defrancq, Eric
Elias, Benjamin
UCL - SST/IMCN/MOST - Molecular Chemistry, Materials and Catalysis
Gillard, Martin
Piraux, Guillaume
Daenen, Martin
Abraham, Michael
Troian-Gautier, Ludovic
Bar, Laure
Bonnet, Hugues
Loiseau, Frédérique
Jamet, Hélène
Dejeu, Jérome
Defrancq, Eric
Elias, Benjamin
Source :
Chemistry – A European Journal, , p. e202202251 (2022)
Publication Year :
2022

Abstract

Photosensitizers that gather high photo-oxidizing power and strong visible light absorption are of great interest in the development of new photo-chemotherapeutics. Indeed, such compounds constitute attractive candidates for the design of type I photosensitizers that are not dependent on the presence of oxygen. In this paper, we report on the synthesis and studies of new ruthenium(II) complexes that display strong visible light absorption and can oxidize guanine residues under visible light irradiation, as evidenced by nanosecond transient absorption spectroscopy. The reported compounds also tightly bind to G-quadruplex DNA structures from the human telomeric sequence (TTAGGG repeat). The kinetic and thermodynamic parameters of the interaction of these Ru(II) complexes with G-quadruplex and duplex DNA were studied thanks to luminescence titrations and bio-layer interferometry measurements, which revealed higher affinities towards the non-canonical G-quadruplex architecture. Docking experiments and non-covalent ionic analysis allowed to gain information on the mode and the strength of the interaction of the compounds towards G-quadruplex and duplex DNA. The different studies emphasize the substantial influence of the position and the number of non-chelating nitrogen atoms on the interaction with both types of DNA secondary structures.

Details

Database :
OAIster
Journal :
Chemistry – A European Journal, , p. e202202251 (2022)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1372947554
Document Type :
Electronic Resource