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Dimeric Metal-Salphen Complexes Which Target Multimeric G-Quadruplex DNA

[Image: see text] G-Quadruplex DNA structures have attracted increasing attention due to their biological roles and potential as targets for the development of new drugs. While most guanine-rich sequences in the genome have the potential to form monomeric G-quadruplexes, certain sequences have enoug...

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Detalles Bibliográficos
Autores principales: Kench, Timothy, Rakers, Viktoria, Bouzada, David, Gomez-González, Jacobo, Robinson, Jenna, Kuimova, Marina K., Vázquez López, Miguel, Vázquez, M. Eugenio, Vilar, Ramon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197068/
https://www.ncbi.nlm.nih.gov/pubmed/37119235
http://dx.doi.org/10.1021/acs.bioconjchem.3c00114
Descripción
Sumario:[Image: see text] G-Quadruplex DNA structures have attracted increasing attention due to their biological roles and potential as targets for the development of new drugs. While most guanine-rich sequences in the genome have the potential to form monomeric G-quadruplexes, certain sequences have enough guanine-tracks to give rise to multimeric quadruplexes. One of these sequences is the human telomere where tandem repeats of TTAGGG can lead to the formation of two or more adjacent G-quadruplexes. Herein we report on the modular synthesis via click chemistry of dimeric metal-salphen complexes (with Ni(II) and Pt(II)) bridged by either polyether or peptide linkers. We show by circular dichroism (CD) spectroscopy that they generally have higher selectivity for dimeric vs monomeric G-quadruplexes. The emissive properties of the Pt(II)-salphen dimeric complexes have been used to study their interactions with monomeric and dimeric G-quadruplexes in vitro as well as to study their cellular uptake and localization.