AUTHOR=Kotras Clément , Fossépré Mathieu , Roger Maxime , Gervais Virginie , Richeter Sébastien , Gerbier Philippe , Ulrich Sébastien , Surin Mathieu , Clément Sébastien 

TITLE=A Cationic Tetraphenylethene as a Light-Up Supramolecular Probe for DNA G-Quadruplexes

JOURNAL=Frontiers in Chemistry

VOLUME=7

YEAR=2019

URL=https://www.frontiersin.org/journals/chemistry/articles/10.3389/fchem.2019.00493

DOI=10.3389/fchem.2019.00493

ISSN=2296-2646

ABSTRACT=<p>Guanine-quadruplexes (G4s) are targets for anticancer therapeutics. In this context, human telomeric DNA (HT-DNA) that can fold into G4s sequences are of particular interest, and their stabilization with small molecules through a visualizable process has become a challenge. As a new type of ligand for HT-G4, we designed a tetraimidazolium tetraphenylethene (<bold>TPE-Im</bold>) as a water-soluble light-up G4 probe. We study its G4-binding properties with HT-DNA by UV-Visible absorption, circular dichroism and fluorescence spectroscopies, which provide insights into the interactions between <bold>TPE-Im</bold> and G4-DNA. Remarkably, <bold>TPE-Im</bold> shows a strong fluorescence enhancement and large shifts upon binding to G4, which is valuable for detecting G4s. The association constants for the <bold>TPE-Im</bold>/G4 complex were evaluated in different solution conditions via isothermal titration calorimetry (ITC), and its binding modes were explored by molecular modeling showing a groove-binding mechanism. The stabilization of G4 by <bold>TPE-Im</bold> has been assessed by Fluorescence Resonance Energy Transfer (FRET) melting assays, which show a strong stabilization (Δ<italic>T</italic><sub>1/2</sub> around +20°C), together with a specificity toward G4 with respect to double-stranded DNA.</p>