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- W3100237589 abstract "Abstract 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." @default.
- W3100237589 created "2020-11-23" @default.
- W3100237589 creator A5002226557 @default.
- W3100237589 creator A5019499764 @default.
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- W3100237589 creator A5031310964 @default.
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- W3100237589 creator A5059072908 @default.
- W3100237589 creator A5068460541 @default.
- W3100237589 creator A5087382168 @default.
- W3100237589 creator A5089780593 @default.
- W3100237589 date "2020-11-16" @default.
- W3100237589 modified "2023-10-13" @default.
- W3100237589 title "Disclosing the actual efficiency of G-quadruplex-DNA–disrupting small molecules" @default.
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