Probing A-form DNA: A fluorescent aminosugar probe and dual recognition by anthraquinone-neomycin conjugates.

Bioorg Med Chem

NUBAD, LLC, Greenville, SC 29607, USA; Department of Chemistry, Clemson University, Clemson, SC 29634, USA. Electronic address:

Published: February 2017

AI Article Synopsis

  • Nucleic acids, like DNA, have various hydrogen-bonded structures that play important roles in cellular functions and their architecture can vary based on sequence.
  • A novel fluorescent displacement assay was developed using a fluorescein-neomycin conjugate to study A-form DNA without disrupting its natural structure, unlike intercalating dyes.
  • This assay can identify compounds that bind to duplex DNA and also analyze the structural characteristics of specific DNA sequences, making it suitable for large-scale screening of potential binding compounds.

Article Abstract

Nucleic acids adopt a broad array of hydrogen-bonded structures that enable their diverse roles in the cell; even the familiar DNA double helix displays subtle architectural nuances that are sequence dependent. While there have been many approaches for recognition of B-form nucleic acids, A-form DNA recognition has lagged behind. Here, using a tight binding fluorescein-neomycin (F-neo) conjugate that can probe the electrostatic environment of A-form DNA major groove, we developed a fluorescent displacement assay to be used as a screen for DNA duplex-binding compounds. As opposed to intercalating dyes that can significantly perturb DNA structure, the groove binding F-neo allows the probing of native DNA conformation. In combination with the assay development and probing of DNA grooves, we also report the synthesis and binding of a series of neomycin-anthraquinone conjugates, two units with a known preference for binding GC rich DNA. The assay can be used to identify duplex DNA-binding compounds, as well as probe structural features of a target DNA duplex, and can easily be scaled up for high throughput screening of compound libraries.

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http://dx.doi.org/10.1016/j.bmc.2016.11.003DOI Listing

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