| Literature DB >> 33415794 |
Nada Farag1, Rosanna Mattossovich2, Rosa Merlo2, Łukasz Nierzwicki3, Giulia Palermo3,4, Alessandro Porchetta1, Giuseppe Perugino2, Francesco Ricci1.
Abstract
We present a new class of DNA-based nanoswitches that, upon enzymatic repair, could undergo a conformational change mechanism leading to a change in fluorescent signal. Such folding-upon-repair DNA nanoswitches are synthetic DNA sequences containing O6 -methyl-guanine (O6 -MeG) nucleobases and labelled with a fluorophore/quencher optical pair. The nanoswitches are rationally designed so that only upon enzymatic demethylation of the O6 -MeG nucleobases they can form stable intramolecular Hoogsteen interactions and fold into an optically active triplex DNA structure. We have first characterized the folding mechanism induced by the enzymatic repair activity through fluorescent experiments and Molecular Dynamics simulations. We then demonstrated that the folding-upon-repair DNA nanoswitches are suitable and specific substrates for different methyltransferase enzymes including the human homologue (hMGMT) and they allow the screening of novel potential methyltransferase inhibitors.Entities:
Keywords: DNA nanoswitches; DNA nanotechnology; DNA repair enzymes; conformational change mechanism; triplex DNA
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Year: 2021 PMID: 33415794 PMCID: PMC8783695 DOI: 10.1002/anie.202016223
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336