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Folding-upon-Repair DNA Nanoswitches for Monitoring the Activity of DNA Repair Enzymes.
Farag, Nada; Mattossovich, Rosanna; Merlo, Rosa; Nierzwicki, Lukasz; Palermo, Giulia; Porchetta, Alessandro; Perugino, Giuseppe; Ricci, Francesco.
Afiliación
  • Farag N; Department of Chemistry, University of Rome Tor Vergata, Via della Ricerca Scientifica, 00133, Rome, Italy.
  • Mattossovich R; Institute of Biosciences and BioResources, National Research Council of Italy, Via Pietro Castellino 111, 80131, Naples, Italy.
  • Merlo R; Institute of Biosciences and BioResources, National Research Council of Italy, Via Pietro Castellino 111, 80131, Naples, Italy.
  • Nierzwicki L; Department of Bioengineering, University of California Riverside, 900 University Avenue, Riverside, CA, 52512, USA.
  • Palermo G; Department of Bioengineering, University of California Riverside, 900 University Avenue, Riverside, CA, 52512, USA.
  • Porchetta A; Department of Chemistry, University of California Riverside, 900 University Avenue, Riverside, CA, 52512, USA.
  • Perugino G; Department of Chemistry, University of Rome Tor Vergata, Via della Ricerca Scientifica, 00133, Rome, Italy.
  • Ricci F; Institute of Biosciences and BioResources, National Research Council of Italy, Via Pietro Castellino 111, 80131, Naples, Italy.
Angew Chem Int Ed Engl ; 60(13): 7283-7289, 2021 03 22.
Article en En | MEDLINE | ID: mdl-33415794
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / O(6)-Metilguanina-ADN Metiltransferasa / Nanotecnología Límite: Humans Idioma: En Revista: Angew Chem Int Ed Engl Año: 2021 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / O(6)-Metilguanina-ADN Metiltransferasa / Nanotecnología Límite: Humans Idioma: En Revista: Angew Chem Int Ed Engl Año: 2021 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Alemania