Progress and prospects of pyrrole-imidazole polyamide-fluorophore conjugates as sequence-selective DNA probes

Chembiochem. 2012 Oct 15;13(15):2170-85. doi: 10.1002/cbic.201200451. Epub 2012 Sep 28.

Abstract

Recently, the versatility of N-methylpyrrole (Py)-N-methylimidazole (Im) polyamide conjugates, which have been developed from the DNA-binding antibiotics distamycin A and netropsin, has been shown. These synthetic small molecules can permeate cells to bind with duplex DNA in a sequence-specific manner, and hence can influence gene expression in vivo. Accordingly, several reports demonstrating the sequence specificity and biological activity of Py-Im polyamides have accumulated. However, the benefits of Py-Im polyamides, in particular those conjugated with fluorophores, has been overlooked. Moreover, clear directions for the employment of these attractive artificial small molecules have not yet been shown. Here, we present a detailed overview of the current and prospective applications of Py-Im polyamide-fluorophore conjugates, including sequence-specific recognition with fluorescence emission properties, and their potential roles in biological imaging.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • DNA / analysis*
  • DNA Probes / chemistry*
  • Fluorescent Dyes / chemistry*
  • Humans
  • Imidazoles / chemistry*
  • Models, Molecular
  • Nylons / chemistry*
  • Optical Imaging / methods
  • Pyrroles / chemistry*

Substances

  • DNA Probes
  • Fluorescent Dyes
  • Imidazoles
  • Nylons
  • Pyrroles
  • DNA