New environment-sensitive multichannel DNA fluorescent label for investigation of the protein-DNA interactions

PLoS One. 2014 Jun 12;9(6):e100007. doi: 10.1371/journal.pone.0100007. eCollection 2014.

Abstract

Here, we report the study of a new multichannel DNA fluorescent base analogue 3-hydroxychromone (3HC) to evaluate its suitability as a fluorescent reporter probe of structural transitions during protein-DNA interactions and its comparison with the current commercially available 2-aminopurine (aPu), pyrrolocytosine (Cpy) and 1,3-diaza-2-oxophenoxazine (tCO). For this purpose, fluorescent base analogues were incorporated into DNA helix on the opposite or on the 5'-side of the damaged nucleoside 5,6-dihydrouridine (DHU), which is specifically recognized and removed by Endonuclease VIII. These fluorophores demonstrated different sensitivities to the DNA helix conformational changes. The highest sensitivity and the most detailed information about the conformational changes of DNA induced by protein binding and processing were obtained using the 3HC probe. The application of this new artificial fluorescent DNA base is a very useful tool for the studies of complex mechanisms of protein-DNA interactions. Using 3HC biosensor, the kinetic mechanism of Endonuclease VIII action was specified.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Chromones / chemistry*
  • DNA / chemistry*
  • DNA / metabolism
  • Deoxyribonuclease (Pyrimidine Dimer) / chemistry*
  • Deoxyribonuclease (Pyrimidine Dimer) / metabolism
  • Escherichia coli Proteins / chemistry*
  • Escherichia coli Proteins / metabolism
  • Fluorescent Dyes / chemistry*
  • Molecular Dynamics Simulation
  • Molecular Sequence Data
  • Protein Binding

Substances

  • 3-hydroxychromone
  • Chromones
  • Escherichia coli Proteins
  • Fluorescent Dyes
  • DNA
  • Deoxyribonuclease (Pyrimidine Dimer)

Grants and funding

The study was supported by the Program of the Russian Academy of Sciences “Molecular & Cell Biology” (No 6.11), the Grants from Russian Foundation for Basic Research (12-04-00135, 14-04-00531, 13-04-00013 and 14-04-31174) and Russian Ministry of Education and Science (SS-1205.2014.4 and SP-4012.2013.4), the Grant from Russian Scientific Foundation (14-14-00063). The ANR (ANR-12-BS08-0003-02) and the FRM (DCM20111223038) are thanked for financial support and grant for N.P.F.B. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.