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

• Published in: JACS Au Vol. 2; no. 7; pp. 1588 - 1595
• Main Authors: Rota Sperti, Francesco, Dupouy, Baptiste, Mitteaux, Jérémie, Pipier, Angélique, Pirrotta, Marc, Chéron, Nicolas, Valverde, Ibai E., Monchaud, David
• Format: Journal Article
• Language: English
• Published: American Chemical Society 25.07.2022; ACS Publications
• Subjects: Chemical Sciences; Genetics; Letter; Life Sciences; ligands; affinity capture; DNA damage; optical imaging; G-quadruplex
• ISSN: 2691-3704; 2691-3704
• DOI: 10.1021/jacsau.2c00082

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.