Enantiospecific recognition of DNA sequences by a proflavine Tröger base

Biochem Biophys Res Commun. 2000 Jul 5;273(2):681-5. doi: 10.1006/bbrc.2000.2997.

Abstract

The DNA interaction of a chiral Tröger base derived from proflavine was investigated by DNA melting temperature measurements and complementary biochemical assays. DNase I footprinting experiments demonstrate that the binding of the proflavine-based Tröger base is both enantio- and sequence-specific. The (+)-isomer poorly interacts with DNA in a non-sequence-selective fashion. In sharp contrast, the corresponding (-)-isomer recognizes preferentially certain DNA sequences containing both A. T and G. C base pairs, such as the motifs 5'-GTT. AAC and 5'-ATGA. TCAT. This is the first experimental demonstration that acridine-type Tröger bases can be used for enantiospecific recognition of DNA sequences.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Pairing
  • Base Sequence
  • Binding Sites
  • Bridged-Ring Compounds / chemistry
  • Bridged-Ring Compounds / metabolism
  • Cattle
  • DNA / chemistry
  • DNA / genetics
  • DNA / metabolism*
  • DNA Footprinting
  • In Vitro Techniques
  • Proflavine / chemistry*
  • Proflavine / metabolism*
  • Stereoisomerism

Substances

  • Bridged-Ring Compounds
  • DNA
  • Proflavine