Fiche publication
Date publication
mars 2015
Journal
Chemical communications (Cambridge, England)
Auteurs
Membres identifiés du Cancéropôle Est :
Dr DZIUBA Dmytro
Tous les auteurs :
Dziuba D, Pohl R, Hocek M
Lien Pubmed
Résumé
Viscosity-sensitive fluorophores, fluorescent molecular rotors based on aminobenzylidene-cyanoacetamide moiety, were tethered to 2'-deoxycytidine triphosphate via a propargylamine linker and incorporated into DNA by polymerases in primer extension, nicking enzyme amplification or PCR. DNA probes incorporating modified nucleosides show a light-up response upon binding to a protein.
Mots clés
Aniline Compounds, chemistry, Benzylidene Compounds, chemistry, DNA, chemistry, DNA-Binding Proteins, chemistry, DNA-Directed DNA Polymerase, metabolism, Fluorescent Dyes, chemistry, Molecular Structure, Nitriles, chemistry, Protein Binding
Référence
Chem Commun (Camb). 2015 03 21;51(23):4880-2