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A red light-triggered chemical tool for sequence-specific alkylation of G-quadruplex and I-motif DNA

The importance of non-canonical DNA structures such as G-quadruplexes (G4) and intercalating-motifs (iMs) in the fine regulation of a variety of cellular processes has been recently demonstrated. As the crucial roles of these structures are being unravelled, it is becoming more and more important to...

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Autores principales: Cadoni, Enrico, De Paepe, Lessandro, Colpaert, Gertjan, Tack, Ruben, Waegeman, Dries, Manicardi, Alex, Madder, Annemieke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201448/
https://www.ncbi.nlm.nih.gov/pubmed/36971129
http://dx.doi.org/10.1093/nar/gkad189
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author Cadoni, Enrico
De Paepe, Lessandro
Colpaert, Gertjan
Tack, Ruben
Waegeman, Dries
Manicardi, Alex
Madder, Annemieke
author_facet Cadoni, Enrico
De Paepe, Lessandro
Colpaert, Gertjan
Tack, Ruben
Waegeman, Dries
Manicardi, Alex
Madder, Annemieke
author_sort Cadoni, Enrico
collection PubMed
description The importance of non-canonical DNA structures such as G-quadruplexes (G4) and intercalating-motifs (iMs) in the fine regulation of a variety of cellular processes has been recently demonstrated. As the crucial roles of these structures are being unravelled, it is becoming more and more important to develop tools that allow targeting these structures with the highest possible specificity. While targeting methodologies have been reported for G4s, this is not the case for iMs, as evidenced by the limited number of specific ligands able to bind the latter and the total absence of selective alkylating agents for their covalent targeting. Furthermore, strategies for the sequence-specific covalent targeting of G4s and iMs have not been reported thus far. Herein, we describe a simple methodology to achieve sequence-specific covalent targeting of G4 and iM DNA structures based on the combination of (i) a peptide nucleic acid (PNA) recognizing a specific sequence of interest, (ii) a pro-reactive moiety enabling a controlled alkylation reaction, and (iii) a G4 or iM ligand orienting the alkylating warhead to the reactive residues. This multi-component system allows for the targeting of specific G4 or iM sequences of interest in the presence of competing DNA sequences and under biologically relevant conditions.
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spelling pubmed-102014482023-05-23 A red light-triggered chemical tool for sequence-specific alkylation of G-quadruplex and I-motif DNA Cadoni, Enrico De Paepe, Lessandro Colpaert, Gertjan Tack, Ruben Waegeman, Dries Manicardi, Alex Madder, Annemieke Nucleic Acids Res Chemical Biology and Nucleic Acid Chemistry The importance of non-canonical DNA structures such as G-quadruplexes (G4) and intercalating-motifs (iMs) in the fine regulation of a variety of cellular processes has been recently demonstrated. As the crucial roles of these structures are being unravelled, it is becoming more and more important to develop tools that allow targeting these structures with the highest possible specificity. While targeting methodologies have been reported for G4s, this is not the case for iMs, as evidenced by the limited number of specific ligands able to bind the latter and the total absence of selective alkylating agents for their covalent targeting. Furthermore, strategies for the sequence-specific covalent targeting of G4s and iMs have not been reported thus far. Herein, we describe a simple methodology to achieve sequence-specific covalent targeting of G4 and iM DNA structures based on the combination of (i) a peptide nucleic acid (PNA) recognizing a specific sequence of interest, (ii) a pro-reactive moiety enabling a controlled alkylation reaction, and (iii) a G4 or iM ligand orienting the alkylating warhead to the reactive residues. This multi-component system allows for the targeting of specific G4 or iM sequences of interest in the presence of competing DNA sequences and under biologically relevant conditions. Oxford University Press 2023-03-27 /pmc/articles/PMC10201448/ /pubmed/36971129 http://dx.doi.org/10.1093/nar/gkad189 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Chemical Biology and Nucleic Acid Chemistry
Cadoni, Enrico
De Paepe, Lessandro
Colpaert, Gertjan
Tack, Ruben
Waegeman, Dries
Manicardi, Alex
Madder, Annemieke
A red light-triggered chemical tool for sequence-specific alkylation of G-quadruplex and I-motif DNA
title A red light-triggered chemical tool for sequence-specific alkylation of G-quadruplex and I-motif DNA
title_full A red light-triggered chemical tool for sequence-specific alkylation of G-quadruplex and I-motif DNA
title_fullStr A red light-triggered chemical tool for sequence-specific alkylation of G-quadruplex and I-motif DNA
title_full_unstemmed A red light-triggered chemical tool for sequence-specific alkylation of G-quadruplex and I-motif DNA
title_short A red light-triggered chemical tool for sequence-specific alkylation of G-quadruplex and I-motif DNA
title_sort red light-triggered chemical tool for sequence-specific alkylation of g-quadruplex and i-motif dna
topic Chemical Biology and Nucleic Acid Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201448/
https://www.ncbi.nlm.nih.gov/pubmed/36971129
http://dx.doi.org/10.1093/nar/gkad189
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