Novel porphyrin-daunomycin hybrids: synthesis and preferential binding to G-quadruplexes over i-motif

Spectrochim Acta A Mol Biomol Spectrosc. 2015 Feb 25:137:227-35. doi: 10.1016/j.saa.2014.08.123. Epub 2014 Sep 4.

Abstract

Encouraged by the enormous importance attributed to the structure and function of human telomeric DNA, herein we focused our attention on the interaction of a serious of newly prepared porphyrin-daunomycin (Por-DNR) hybrids with the guanine-rich single-strand oligomer (G4) and the complementary cytosine-rich strand (i-motif). Various spectral methods such as absorption and fluorescence titration, surface-enhanced Raman and circular dichroism spectrum were integrated in the experiment and it was found that these Por-DNR hybrids could serve as prominent molecules to recognize G4 and i-motif. What is more, interesting results were obtained that the hybrids with longer flexible links are more favorable in binding with both G4 and i-motif than the hybrid with shorter linkage. These Por-DNR hybrids may help to develop new ideas in the research of human telomeric DNA with small molecules.

Keywords: G-quadruplexes; Porphyrin–daunomycin hybrids; i-Motif.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Absorption, Physicochemical
  • Binding, Competitive
  • Buffers
  • Circular Dichroism
  • Daunorubicin / chemical synthesis*
  • Daunorubicin / chemistry
  • Daunorubicin / metabolism*
  • Ethidium / metabolism
  • G-Quadruplexes*
  • Nucleic Acid Denaturation
  • Nucleotide Motifs*
  • Porphyrins / chemical synthesis*
  • Porphyrins / chemistry
  • Porphyrins / metabolism*
  • Spectrometry, Fluorescence
  • Spectrum Analysis, Raman
  • Temperature

Substances

  • Buffers
  • Porphyrins
  • Ethidium
  • Daunorubicin