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Progress and Prospects of Pyrrole-Imidazole Polyamide-Fluorophore Conjugates as Sequence-Selective DNA Probes

Journal

CHEMBIOCHEM
Volume 13, Issue 15, Pages 2170-2185

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.201200451

Keywords

cellular and nuclear localization; DNA; dyes; pigments; fluorescent probes; nucleic acids; pyrrole-imidazole polyamides

Funding

  1. Japan Science and Technology Agency (JST)-CREST
  2. global COE program from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan

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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 polyamidefluorophore conjugates, including sequence-specific recognition with fluorescence emission properties, and their potential roles in biological imaging.

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