Interaction between double helix DNA fragments and a new topopyrone acting as human topoisomerase I poison

Bioorg Med Chem. 2009 Jan 15;17(2):484-91. doi: 10.1016/j.bmc.2008.12.005. Epub 2008 Dec 10.

Abstract

A water soluble derivative (2) of topopyrones was selected for NMR studies directed to elucidate the mode of binding with specific oligonucleotides. Topopyrone 2 can intercalate into the CG base pairs, but the residence time into the double helix is very short and a fast chemical exchange averaging occurs at room temperature between the free and bound species. The equilibria involved become slow below room temperature, thus allowing to measure a mean lifetime of the complex of ca. 7 ms at 15 degrees C. Structural models of the complex with d(CGTACG)(2) were developed on the basis of DOSY, 2D NOESY and (31)P NMR experiments. Topopyrone 2 presents a strong tendency to self-associate. In the presence of oligonucleotide a certain number of ligand molecules are found to externally stack to the double-helix, in addition to a small fraction of the same ligand intercalated. The external binding to the ionic surface of the phosphoribose chains may thus represents the first step of the intercalation process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anthraquinones / chemistry*
  • Anthraquinones / pharmacology
  • Base Sequence
  • Binding Sites
  • DNA / chemistry*
  • DNA / metabolism
  • Humans
  • Intercalating Agents
  • Magnetic Resonance Spectroscopy
  • Nucleic Acid Conformation
  • Pyrones / chemistry*
  • Pyrones / pharmacology
  • Solubility
  • Topoisomerase I Inhibitors*

Substances

  • Anthraquinones
  • Intercalating Agents
  • Pyrones
  • Topoisomerase I Inhibitors
  • DNA