Binding of DNA by a dinitro-diester calix[4]arene: Denaturation and condensation of DNA

F. J. Ostos, J. A. Lebron, M. L. Moyá, M. Deasy, P. López-Cornejo

    Research output: Contribution to journalArticlepeer-review

    Abstract

    A study of a dinitro-diester calix[4]arene (5,17-(3-nitrobenzylideneamino)-11,23-di-tert-butyl-25,27-diethoxycarbonyl methyleneoxy-26,28-dihydroxycalix[4]arene) interaction with calf-thymus DNA was carried out using several techniques. The measurements were done at various molar ratios X=[calixarene]/[DNA]. Results show diverse changes in the DNA conformation depending on the X value. Thus, at low macrocycle concentrations, the calixarene binds to the polynucleotide. This interaction, mainly in groove mode, weakens the hydrogen bonds between base pairs of the helix inducing denaturation of the double strands, as well as condensation of the macromolecule, from an extended coil state to a globular state. An opposite effect is observed at X molar ratios higher than 0.07. The de-condensation of DNA happens, that is, the transition from a compact state to a more extended conformation, probably due to the stacking of calixarene molecules in the solution. Results also show the importance of making a proper choice of the system under consideration.

    Original languageEnglish
    Pages (from-to)65-72
    Number of pages8
    JournalColloids and Surfaces B: Biointerfaces
    Volume127
    DOIs
    Publication statusPublished - 1 Mar 2015

    Keywords

    • Calixarene
    • Condensation
    • DNA
    • Denaturation
    • Gene therapy
    • Non-covalent interactions

    Fingerprint

    Dive into the research topics of 'Binding of DNA by a dinitro-diester calix[4]arene: Denaturation and condensation of DNA'. Together they form a unique fingerprint.

    Cite this