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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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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 |
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author | Kench, Timothy Rakers, Viktoria Bouzada, David Gomez-González, Jacobo Robinson, Jenna Kuimova, Marina K. Vázquez López, Miguel Vázquez, M. Eugenio Vilar, Ramon |
author_facet | Kench, Timothy Rakers, Viktoria Bouzada, David Gomez-González, Jacobo Robinson, Jenna Kuimova, Marina K. Vázquez López, Miguel Vázquez, M. Eugenio Vilar, Ramon |
author_sort | Kench, Timothy |
collection | PubMed |
description | [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. |
format | Online Article Text |
id | pubmed-10197068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-101970682023-05-20 Dimeric Metal-Salphen Complexes Which Target Multimeric G-Quadruplex DNA Kench, Timothy Rakers, Viktoria Bouzada, David Gomez-González, Jacobo Robinson, Jenna Kuimova, Marina K. Vázquez López, Miguel Vázquez, M. Eugenio Vilar, Ramon Bioconjug Chem [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. American Chemical Society 2023-04-29 /pmc/articles/PMC10197068/ /pubmed/37119235 http://dx.doi.org/10.1021/acs.bioconjchem.3c00114 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Kench, Timothy Rakers, Viktoria Bouzada, David Gomez-González, Jacobo Robinson, Jenna Kuimova, Marina K. Vázquez López, Miguel Vázquez, M. Eugenio Vilar, Ramon Dimeric Metal-Salphen Complexes Which Target Multimeric G-Quadruplex DNA |
title | Dimeric
Metal-Salphen Complexes Which Target Multimeric
G-Quadruplex DNA |
title_full | Dimeric
Metal-Salphen Complexes Which Target Multimeric
G-Quadruplex DNA |
title_fullStr | Dimeric
Metal-Salphen Complexes Which Target Multimeric
G-Quadruplex DNA |
title_full_unstemmed | Dimeric
Metal-Salphen Complexes Which Target Multimeric
G-Quadruplex DNA |
title_short | Dimeric
Metal-Salphen Complexes Which Target Multimeric
G-Quadruplex DNA |
title_sort | dimeric
metal-salphen complexes which target multimeric
g-quadruplex dna |
url | 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 |
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