Novel high-throughput electrochemiluminescent assay for identification of human tyrosyl-DNA phosphodiesterase (Tdp1) inhibitors and characterization of furamidine (NSC 305831) as an inhibitor of Tdp1

Nucleic Acids Res. 2007;35(13):4474-84. doi: 10.1093/nar/gkm463. Epub 2007 Jun 18.

Abstract

By enzymatically hydrolyzing the terminal phosphodiester bond at the 3'-ends of DNA breaks, tyrosyl-DNA phosphodiesterase (Tdp1) repairs topoisomerase-DNA covalent complexes and processes the DNA ends for DNA repair. To identify novel Tdp1 inhibitors, we developed a high-throughput assay that uses electrochemiluminescent (ECL) substrates. Subsequent to screening of 1981 compounds from the 'diversity set' of the NCI-Developmental Therapeutics Program, here we report that furamidine inhibits Tdp1 at low micromolar concentrations. Inhibition of Tdp1 by furamidine is effective both with single- and double-stranded substrates but is slightly stronger with the duplex DNA. Surface plasmon resonance studies show that furamidine binds both single- and double-stranded DNA, though more weakly with the single-stranded substrate DNA. Thus, the inhibition of Tdp1 activity could in part be due to the binding of furamidine to DNA. However, the inhibition of Tdp1 by furamidine is independent of the substrate DNA sequence. The kinetics of Tdp1 inhibition by furamidine was influenced by the drug to enzyme ratio and duration of the reaction. Comparison with related dications shows that furamidine inhibits Tdp1 more effectively than berenil, while pentamidine was inactive. Thus, furamidine represents the most potent Tdp1 inhibitor reported to date.

Publication types

  • Evaluation Study
  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural

MeSH terms

  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Benzamidines / chemistry
  • Benzamidines / pharmacology*
  • DNA / chemistry
  • DNA / metabolism
  • DNA, Single-Stranded / metabolism
  • Diminazene / analogs & derivatives
  • Diminazene / chemistry
  • Diminazene / pharmacology
  • Drug Evaluation, Preclinical / methods
  • Electrochemistry
  • Humans
  • Kinetics
  • Luminescent Measurements*
  • Pentamidine / chemistry
  • Pentamidine / pharmacology
  • Phosphodiesterase Inhibitors / chemistry
  • Phosphodiesterase Inhibitors / pharmacology*
  • Phosphoric Diester Hydrolases / metabolism*
  • Thymidine / chemistry

Substances

  • Antineoplastic Agents
  • Benzamidines
  • DNA, Single-Stranded
  • Phosphodiesterase Inhibitors
  • Pentamidine
  • furamidine
  • DNA
  • Phosphoric Diester Hydrolases
  • TDP1 protein, human
  • diminazene aceturate
  • Thymidine
  • Diminazene