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Click-Chemistry-Based Biomimetic Ligands Efficiently Capture G-Quadruplexes In Vitro and Help Localize Them at DNA Damage Sites in Human Cells

[Image: see text] Interrogating G-quadruplex (G4) biology at its deepest roots in human cells relies on the design, synthesis, and use of ever smarter molecular tools. Here, we demonstrate the versatility of biomimetic G4 ligands referred to as TASQ (template assembled synthetic G-quartet) in which...

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Autores principales: Rota Sperti, Francesco, Dupouy, Baptiste, Mitteaux, Jérémie, Pipier, Angélique, Pirrotta, Marc, Chéron, Nicolas, Valverde, Ibai E., Monchaud, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327089/
https://www.ncbi.nlm.nih.gov/pubmed/35911444
http://dx.doi.org/10.1021/jacsau.2c00082
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author Rota Sperti, Francesco
Dupouy, Baptiste
Mitteaux, Jérémie
Pipier, Angélique
Pirrotta, Marc
Chéron, Nicolas
Valverde, Ibai E.
Monchaud, David
author_facet Rota Sperti, Francesco
Dupouy, Baptiste
Mitteaux, Jérémie
Pipier, Angélique
Pirrotta, Marc
Chéron, Nicolas
Valverde, Ibai E.
Monchaud, David
author_sort Rota Sperti, Francesco
collection PubMed
description [Image: see text] Interrogating G-quadruplex (G4) biology at its deepest roots in human cells relies on the design, synthesis, and use of ever smarter molecular tools. Here, we demonstrate the versatility of biomimetic G4 ligands referred to as TASQ (template assembled synthetic G-quartet) in which a biotin handle was incorporated for G4-focused chemical biology investigations. We have rethought the biotinylated TASQ design to make it readily chemically accessible via an efficient click-chemistry-based strategy. The resulting biotinylated, triazole-assembled TASQ, or BioTriazoTASQ, was thus shown to efficiently isolate both DNA and RNA G4s from solution by affinity purification protocols, for identification purposes. Its versatility was then further demonstrated by optical imaging that provided unique mechanistic insights into the actual strategic relevance of G4-targeting strategies, showing that ligand-stabilized G4 sites colocalize with and, thus, are responsible for DNA damage foci in human cells.
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spelling pubmed-93270892022-07-28 Click-Chemistry-Based Biomimetic Ligands Efficiently Capture G-Quadruplexes In Vitro and Help Localize Them at DNA Damage Sites in Human Cells Rota Sperti, Francesco Dupouy, Baptiste Mitteaux, Jérémie Pipier, Angélique Pirrotta, Marc Chéron, Nicolas Valverde, Ibai E. Monchaud, David JACS Au [Image: see text] Interrogating G-quadruplex (G4) biology at its deepest roots in human cells relies on the design, synthesis, and use of ever smarter molecular tools. Here, we demonstrate the versatility of biomimetic G4 ligands referred to as TASQ (template assembled synthetic G-quartet) in which a biotin handle was incorporated for G4-focused chemical biology investigations. We have rethought the biotinylated TASQ design to make it readily chemically accessible via an efficient click-chemistry-based strategy. The resulting biotinylated, triazole-assembled TASQ, or BioTriazoTASQ, was thus shown to efficiently isolate both DNA and RNA G4s from solution by affinity purification protocols, for identification purposes. Its versatility was then further demonstrated by optical imaging that provided unique mechanistic insights into the actual strategic relevance of G4-targeting strategies, showing that ligand-stabilized G4 sites colocalize with and, thus, are responsible for DNA damage foci in human cells. American Chemical Society 2022-06-17 /pmc/articles/PMC9327089/ /pubmed/35911444 http://dx.doi.org/10.1021/jacsau.2c00082 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Rota Sperti, Francesco
Dupouy, Baptiste
Mitteaux, Jérémie
Pipier, Angélique
Pirrotta, Marc
Chéron, Nicolas
Valverde, Ibai E.
Monchaud, David
Click-Chemistry-Based Biomimetic Ligands Efficiently Capture G-Quadruplexes In Vitro and Help Localize Them at DNA Damage Sites in Human Cells
title Click-Chemistry-Based Biomimetic Ligands Efficiently Capture G-Quadruplexes In Vitro and Help Localize Them at DNA Damage Sites in Human Cells
title_full Click-Chemistry-Based Biomimetic Ligands Efficiently Capture G-Quadruplexes In Vitro and Help Localize Them at DNA Damage Sites in Human Cells
title_fullStr Click-Chemistry-Based Biomimetic Ligands Efficiently Capture G-Quadruplexes In Vitro and Help Localize Them at DNA Damage Sites in Human Cells
title_full_unstemmed Click-Chemistry-Based Biomimetic Ligands Efficiently Capture G-Quadruplexes In Vitro and Help Localize Them at DNA Damage Sites in Human Cells
title_short Click-Chemistry-Based Biomimetic Ligands Efficiently Capture G-Quadruplexes In Vitro and Help Localize Them at DNA Damage Sites in Human Cells
title_sort click-chemistry-based biomimetic ligands efficiently capture g-quadruplexes in vitro and help localize them at dna damage sites in human cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327089/
https://www.ncbi.nlm.nih.gov/pubmed/35911444
http://dx.doi.org/10.1021/jacsau.2c00082
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