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Probing DNA - transcription factor interactions using single-molecule fluorescence detection in nanofluidic devices

View ORCID ProfileMattia Fontana, View ORCID ProfileŠarūnė Ivanovaitė, View ORCID ProfileSimon Lindhoud, Willy van den Berg, View ORCID ProfileDolf Weijers, View ORCID ProfileJohannes Hohlbein
doi: https://doi.org/10.1101/2021.05.12.443786
Mattia Fontana
aLaboratory of Biophysics, Wageningen University and Research, Stippeneng 4, 6708 WE Wageningen, The Netherlands
bLaboratory of Biochemistry, Wageningen University and Research, Stippeneng 4, 6708 WE Wageningen, The Netherlands
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Šarūnė Ivanovaitė
aLaboratory of Biophysics, Wageningen University and Research, Stippeneng 4, 6708 WE Wageningen, The Netherlands
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Simon Lindhoud
bLaboratory of Biochemistry, Wageningen University and Research, Stippeneng 4, 6708 WE Wageningen, The Netherlands
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Willy van den Berg
bLaboratory of Biochemistry, Wageningen University and Research, Stippeneng 4, 6708 WE Wageningen, The Netherlands
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Dolf Weijers
bLaboratory of Biochemistry, Wageningen University and Research, Stippeneng 4, 6708 WE Wageningen, The Netherlands
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Johannes Hohlbein
bLaboratory of Biochemistry, Wageningen University and Research, Stippeneng 4, 6708 WE Wageningen, The Netherlands
cMicrospectroscopy Research Facility, Wageningen University and Research, Stippeneng 4, 6708 WE Wageningen, The Netherlands
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  • For correspondence: johannes.hohlbein@wur.nl
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Abstract

Single-molecule fluorescence detection offers powerful ways to study biomolecules and their complex interactions. Here, we combine nanofluidic devices and camera-based, single-molecule Förster resonance energy transfer (smFRET) detection to study the interactions between plant transcription factors of the auxin response family (ARF) and DNA oligonucleotides that contain target DNA response elements. In particular, we show that the binding of the unlabelled ARF DNA binding domain (ARF-DBD) to donor and acceptor labelled DNA oligonucleotides can be detected by changes in the FRET efficiency and changes in the diffusion coefficient of the DNA. In addition, our data on fluorescently labelled ARF-DBDs suggest that, at nanomolar concentrations, ARF-DBDs are exclusively present as monomers. In general, the fluidic framework of freely diffusing molecules minimizes potential surface-induced artifacts, enables high-throughput measurements and proved to be instrumental in shedding more light on the interactions between ARF-DBDs monomers and between ARF-DBDs and their DNA response element.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted May 13, 2021.
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Probing DNA - transcription factor interactions using single-molecule fluorescence detection in nanofluidic devices
Mattia Fontana, Šarūnė Ivanovaitė, Simon Lindhoud, Willy van den Berg, Dolf Weijers, Johannes Hohlbein
bioRxiv 2021.05.12.443786; doi: https://doi.org/10.1101/2021.05.12.443786
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Probing DNA - transcription factor interactions using single-molecule fluorescence detection in nanofluidic devices
Mattia Fontana, Šarūnė Ivanovaitė, Simon Lindhoud, Willy van den Berg, Dolf Weijers, Johannes Hohlbein
bioRxiv 2021.05.12.443786; doi: https://doi.org/10.1101/2021.05.12.443786

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