Disclosing the actual efficiency of G-quadruplex-DNA–disrupting small molecules
| Autor: | Alexandra Joubert, Nicolas Desbois, Pauline Lejault, Jean-Baptiste Boulé, Anton Granzhan, Filip Wojciechowski, David Monchaud, Robert H. E. Hudson, Marc Pirrotta, Jeremie Mitteaux, Claude P. Gros |
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| Přispěvatelé: | Structure et Instabilité des Génomes (STRING), Muséum national d'Histoire naturelle (MNHN)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie Moléculaire de l'Université de Bourgogne [Dijon] (ICMUB), Centre National de la Recherche Scientifique (CNRS)-Université de Bourgogne (UB)-Institut de Chimie du CNRS (INC) |
| Rok vydání: | 2020 |
| Předmět: |
0303 health sciences
Computer science Chemical biology [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biology [CHIM.THER]Chemical Sciences/Medicinal Chemistry Computational biology 010402 general chemistry G-quadruplex 01 natural sciences Small molecule In vitro 0104 chemical sciences 03 medical and health sciences chemistry.chemical_compound chemistry DNA 030304 developmental biology |
| Popis: | The quest for small molecules that avidly bind to G-quadruplex-DNA (G4-DNA, or G4), so called G4-ligands, has invigorated the G4 research field from its very inception. Massive efforts have been invested to i- screen or design G4-ligands, ii- evaluate their G4-interacting properties in vitro through a series of now widely accepted and routinely implemented assays, and iii- use them as unique chemical biology tools to interrogate cellular networks that might involve G4s. In sharp contrast, only uncoordinated efforts at developing small molecules aimed at destabilizing G4s have been invested to date, even though it is now recognized that such molecular tools would have tremendous application to neurobiology as many genetic and age-related diseases are caused by an over-representation of G4s, itself caused by a deficiency of G4-resolving enzymes, the G4-helicases. Herein, we report on our double effort to i- develop a reliable in vitro assay to identify molecules able to destabilize G4s, the G4-unfold assay, and ii- fully characterize the first prototype of G4-disrupting small molecule, a phenylpyrrolcytosine (PhpC)-based G-clamp analog. |
| Databáze: | OpenAIRE |
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