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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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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. |
format | Online Article Text |
id | pubmed-9327089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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