Evaluation of simultaneous binding of Chromomycin A3 to the multiple sites of DNA by the new restriction enzyme assay

Bioorg Med Chem Lett. 2018 Jun 1;28(10):1832-1835. doi: 10.1016/j.bmcl.2018.04.013. Epub 2018 Apr 7.

Abstract

Chromomycin A3 (CMA3) is an aureolic acid-type antitumor antibiotic. CMA3 forms dimeric complexes with divalent cations, such as Mg2+, which strongly binds to the GC rich sequence of DNA to inhibit DNA replication and transcription. In this study, the binding property of CMA3 to the DNA sequence containing multiple GC-rich binding sites was investigated by measuring the protection from hydrolysis by the restriction enzymes, AccII and Fnu4HI, for the center of the CGCG site and the 5'-GC↓GGC site, respectively. In contrast to the standard DNase I footprinting method, the DNA substrates are fully hydrolyzed by the restriction enzymes, therefore, the full protection of DNA at all the cleavable sites indicates that CMA3 simultaneously binds to all the binding sites. The restriction enzyme assay has suggested that CMA3 has a high tendency to bind the successive CGCG sites and the CGG repeat.

Keywords: AccII; CGG repeat; Chromomycin A3; Fnu4HI; Multiple CGCG sites.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Binding Sites
  • Chromomycin A3 / chemistry
  • Chromomycin A3 / metabolism*
  • DNA / chemistry
  • DNA / metabolism*
  • Deoxyribonucleases, Type II Site-Specific / metabolism*
  • Dimerization
  • Enzyme Assays
  • Magnesium / chemistry
  • Surface Plasmon Resonance

Substances

  • DNA
  • Chromomycin A3
  • CGCG-specific type II deoxyribonucleases
  • Deoxyribonucleases, Type II Site-Specific
  • Magnesium