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Method Article

Fluorescence Anisotropy to Determine Transcription Factor-DNA Binding Affinity

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July 8th, 2025

In This Article

Abstract

Source: Jung, C. et al., High Sensitivity Measurement of Transcription Factor-DNA Binding Affinities by Competitive Titration Using Fluorescence Microscopy. J. Vis. Exp. (2019).

This video describes high-performance fluorescence anisotropy that helps to monitor the interaction between transcription factors and DNA. The assay monitors the interactions of a fluorophore-labeled DNA molecule with its specific transcription factor by measuring the degree of polarization due to molecular rotation or anisotropy of the fluorophore-labeled DNA.

Protocol

1. Polarization Microscopy

  1. For widefield laser illumination, focus a 638 nm line of a continuous diode laser (40 mW) on the aperture of multimode optical fiber for beam cleanup. Mount a linear polarizer at the output of the fiber to set the polarization of laser light.
  2. Block the excitation component of the emitted light with a dichroic mirror (640 nm cut-off) and a bandpass filter (bandpass 700/75).
  3. Let the fluorescence signal pass through a polarizing beam splitter, which splits the emitted light into its perpendicular and parallel polarized components. Then, focus the non-reflected beam (parallel component) and the r....

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Results

DNA diffusion and fluorescence setup; diagram with laser, agarose gel, objective, and competitor binding.
Figure 1: Schematic depictions of the HIP-FA assay and experimental setup. (a) Gel delivery system for titrating competitor DNA in single wells. (b) HIP-FA microscopy setup.Customized automated widefield microscope with polarized fluorescence light.......

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Disclosures

No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Cy5-labled 16- / 18-bp DNA-oligomersEurofinsCustom synthesis
16- / 18-bp DNA-oligomersEurofinsCustom synthesis
Nile Blue ASigmaN5632-25G
Sensoplate plus microplate 96- or 384-well, PSGreiner655891
384-Well Sensoplate, blackGreiner788896
Agarose, low gelling temperatureSigmaA9414-50G
Sodium Chloride Merck 1.06404.1000
Tween-20 Sigma P1379-1L
Di-Potassium hydrogen phosphate trihydrateMerck 1.05099.1000
Potassium dihydrogen phosphateMerck1.04873.1000
Q-POD ElementMerck MilliporeZMQSP0DE1
Millipak 40 Gamma Gold FilterMerck MilliporeMPGL04GK2
Milli-Q Integral 3 Water Purification SystemMerck MilliporeZRXQ003WW
Quantum TIXMerck MilliporeQTUMOTIX1
DL-DithiothreitolSigma43815-1G
Mastercycler gradientEppendorfZ316083
SafeSeal tube 1.5 mLSarstedt72.706.200
Tube 15 mLSarstedt62.554.502
Multiply-Pro cup 0.2 mL PPSarstedt72.737.002
<strong>MICROSCOPY SETUP:</strong>
Automated widefield microscopeLEICADMI6000
Long distance objectiveLEICAHCX PL FLUOAR L 60x/0.60 N.A. Dry
638 nm line continuous diode laserOmicronPHOxX 638-40, 40mW
Back-illuminated EM-CCD CameraAndoriXon DV897
Dichroic mirrorAHF640nm cut-off
Bandpass filterAHFET bandpass 700/75
Linear polarizerThorlabsLPVISC050-MP2
Polarizing beam splitterThorlabsBS010
Achromatic lensThorlabs200 mm focal length
Multimode optical fiberOptronisFVP600660710
<strong>ROBOTIC SYSTEM:</strong>
Our robotic system includes a Biomek NXP workstation with a 96-channel head and Span-8 pipettors, connected with a servo-shuttle, which are used for all liquid transfer steps. In addition, the system is equipped with orbital shakers and a microplate reader (Paradigm, Molecular device) served by the Span-8 gripperBeckman CoulterBiomek NXP
<strong>SOFTWARE:</strong>
Programming languageNational InstrumentsLabview 9.0
Script for the HiP-FA software available athttps://github.com/ GeneCenterMunich/HiP-FA

Tags

Competitive TitrationFluorophore Labeled DNAUnlabeled Competitor DNAHigh Performance MicroscopyDissociation Constant MeasurementGel Preparation ProtocolZ Stack ImagingHiP FA Software