The Excited State Dynamics of a Mutagenic Cytidine Etheno Adduct Investigated by Combining Time-Resolved Spectroscopy and Quantum Mechanical Calculations

Joint femtosecond fluorescence upconversion experiments and theoretical calculations provide a hitherto unattained degree of characterization and understanding of the mutagenic etheno adduct 3,N4-etheno-2′-deoxycytidine (ϵdC) excited state relaxation. This endogenously formed lesion is attracting gr...

Descripción completa

Detalles Bibliográficos
Autores: Lizondo-Aranda, Paloma, Martínez-Fernández, Lara, Miranda, M. A., Improta, Roberto, Gustavsson, Thomas, Lhiaubet-Vallet, Virginie
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2021
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/284311
Acceso en línea:http://hdl.handle.net/10261/284311
Access Level:acceso abierto
Descripción
Sumario:Joint femtosecond fluorescence upconversion experiments and theoretical calculations provide a hitherto unattained degree of characterization and understanding of the mutagenic etheno adduct 3,N4-etheno-2′-deoxycytidine (ϵdC) excited state relaxation. This endogenously formed lesion is attracting great interest because of its ubiquity in human tissues and its highly mutagenic properties. The ϵdC fluorescence is modified with respect to that of the canonical base dC, with a 3-fold increased lifetime and quantum yield at neutral pH. This behavior is amplified upon protonation of the etheno ring (ϵdCH+). Quantum mechanical calculations show that the lowest energy state ππ*1 is responsible for the fluorescence and that the main nonradiative decay pathway to the ground state goes through an ethene-like conical intersection, involving the out-of-plane motion of the C5 and C6 substituents. This conical intersection is lower in energy than the ππ∗ state (ππ*1) minimum, but a sizable energy barrier explains the increase of ϵdC and ϵdCH+ fluorescence lifetimes with respect to that of dC.

Similares en LA Referencia