4.8 Article

A fluorescence-based helicase assay: application to the screening of G-quadruplex ligands

Journal

NUCLEIC ACIDS RESEARCH
Volume 43, Issue 11, Pages E71-U21

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkv193

Keywords

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Funding

  1. Fondation ARC
  2. Conseil Regional d'Aquitaine
  3. Agence Nationale de la Recherche [ANR-12-IS07-0001, ANR-12-BSV8-0008-01, ANR-10-NANO-04-03]
  4. Institut national de la sante et de la recherche medicale (INSERM)
  5. Agence Nationale de la Recherche (ANR) [ANR-12-IS07-0001] Funding Source: Agence Nationale de la Recherche (ANR)

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Helicases, enzymes that unwind DNA or RNA structure, are present in the cell nucleus and in the mitochondrion. Although the majority of the helicases unwind DNA or RNA duplexes, some of these proteins are known to resolve unusual structures such as G-quadruplexes (G4) in vitro. G4 may form stable barrier to the progression of molecular motors tracking on DNA. Monitoring G4 unwinding by these enzymes may reveal the mechanisms of the enzymes and provides information about the stability of these structures. In the experiments presented herein, we developed a reliable, inexpensive and rapid fluorescence-based technique to monitor the activity of G4 helicases in real time in a 96-well plate format. This system was used to screen a series of G4 structures and G4 binders for their effect on the Pif1 enzyme, a 5' to 3' DNA helicase. This simple assay should be adaptable to analysis of other helicases and G4 structures.

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