Thiazole orange-peptide conjugates: sensitivity of DNA binding to chemical structure

Org Lett. 2004 Feb 19;6(4):517-9. doi: 10.1021/ol0362818.

Abstract

[structure: see text] Derivatives of the highly fluorescent and DNA-binding dye thiazole orange (TO) are described that feature appended peptides. Functionalization of TO can be achieved at either of the endocyclic nitrogens, and the photophysical properties and DNA-binding modes are sensitive to the position of the tethered peptide. A series of TO-peptide conjugates are described, demonstrating the utility of a solid-phase synthesis approach to their preparation and illustrating how the photophysical and DNA-binding properties of the compounds are influenced by chemical structure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Benzothiazoles
  • DNA / chemistry*
  • Fluorescent Dyes / chemistry*
  • Models, Molecular*
  • Molecular Structure
  • Peptides / chemistry*
  • Quinolines
  • Structure-Activity Relationship
  • Thiazoles / chemistry*

Substances

  • Benzothiazoles
  • Fluorescent Dyes
  • Peptides
  • Quinolines
  • Thiazoles
  • thiazole orange
  • DNA