A Redox-Activated G-Quadruplex DNA Binder Based on a Platinum(IV)-Salphen Complex

Angew Chem Int Ed Engl. 2018 Jan 2;57(1):310-313. doi: 10.1002/anie.201709968. Epub 2017 Dec 7.

Abstract

There has been increasing interest in the development of small molecules that can selectively bind to G-quadruplex DNA structures. The latter have been associated with a number of key biological processes and therefore are proposed to be potential targets for drug development. Herein, we report the first example of a reduction-activated G-quadruplex DNA binder. We show that a new octahedral platinum(IV)-salphen complex does not interact with DNA in aqueous media at pH 7.4; however, upon addition of bioreductants such as ascorbic acid or glutathione, the compound is readily reduced to the corresponding square planar platinum(II) complex. In contrast to the parent platinum(IV) complex, the in situ generated platinum(II) complex has good affinity for G-quadruplex DNA.

Keywords: DNA structures; G-quadruplexes; antitumor agents; drug targeting; platinum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ascorbic Acid / chemistry
  • Circular Dichroism
  • Coordination Complexes / chemical synthesis
  • Coordination Complexes / chemistry*
  • DNA / chemistry*
  • G-Quadruplexes*
  • Glutathione / chemistry
  • Hydrogen Peroxide / chemistry
  • Hydrogen-Ion Concentration
  • Ligands
  • Magnetic Resonance Spectroscopy / methods
  • Oxidation-Reduction
  • Phenylenediamines / chemistry*
  • Platinum / chemistry*
  • Water

Substances

  • Coordination Complexes
  • Ligands
  • Phenylenediamines
  • salphen
  • Water
  • Platinum
  • DNA
  • Hydrogen Peroxide
  • Glutathione
  • Ascorbic Acid