Naphthalene Diimides Carrying Two β-Cyclodextrins Prefer Telomere RNA G-Quadruplex Recognition

Molecules. 2022 Jun 23;27(13):4053. doi: 10.3390/molecules27134053.

Abstract

Newly synthesized naphthalene diimide carrying two β-cyclodextrins (NDI-β-CyDs) showed improved specificity for the parallel G-quadruplex structure alongside the hybrid G-quadruplex structure. Specifically, the highest binding affinity of NDI-β-CyDs for the telomere RNA G-quadruplex was observed. The binding simulation indicated that β-cyclodextrins might be available for loop nucleobase inclusion under its complex.

Keywords: DNA; RNA; apyromidinic sites; c-kit; c-myc; naphthalene diimide; nucleobase inclusion; parallel G-quadruplex; telomere RNA; β-cyclodextrins (β-CyDs).

MeSH terms

  • G-Quadruplexes*
  • Imides / chemistry
  • Ligands
  • Naphthalenes
  • RNA
  • Telomere / genetics
  • beta-Cyclodextrins*

Substances

  • Imides
  • Ligands
  • Naphthalenes
  • beta-Cyclodextrins
  • naphthalenediimide
  • RNA