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A general method for the development of multicolor biosensors with large dynamic ranges

View ORCID ProfileLars Hellweg, Anna Edenhofer, Lucas Barck, Magnus-Carsten Huppertz, View ORCID ProfileMichelle. S. Frei, View ORCID ProfileMiroslaw Tarnawski, Andrea Bergner, View ORCID ProfileBirgit Koch, View ORCID ProfileKai Johnsson, View ORCID ProfileJulien Hiblot
doi: https://doi.org/10.1101/2022.11.29.518186
Lars Hellweg
1Department of Chemical Biology, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
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Anna Edenhofer
1Department of Chemical Biology, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
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Lucas Barck
1Department of Chemical Biology, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
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Magnus-Carsten Huppertz
1Department of Chemical Biology, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
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Michelle. S. Frei
1Department of Chemical Biology, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
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Miroslaw Tarnawski
2Protein Expression and Characterization Facility, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
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Andrea Bergner
1Department of Chemical Biology, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
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Birgit Koch
1Department of Chemical Biology, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
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  • ORCID record for Birgit Koch
Kai Johnsson
1Department of Chemical Biology, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
3Institute of Chemical Sciences and Engineering (ISIC), École Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland
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Julien Hiblot
1Department of Chemical Biology, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
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  • ORCID record for Julien Hiblot
  • For correspondence: julien.hiblot@mr.mpg.de
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Abstract

Fluorescent biosensors enable to study cell physiology with spatiotemporal resolution, yet most biosensors suffer from relatively low dynamic ranges. Here, we introduce a family of designed Förster Resonance Energy Transfer (FRET) pairs with near quantitative FRET efficiencies based on the reversible interaction of fluorescent proteins with a fluorescently labeled HaloTag. These FRET pairs enabled the straightforward design of biosensors for calcium, ATP and NAD+ with unprecedented dynamic ranges. The color of each of these biosensors can be readily tuned by either changing the fluorescent protein or the synthetic fluorophore, which enabled to monitor simultaneously free NAD+ in different subcellular compartments upon genotoxic stress. Minimal modifications furthermore allow the readout of these biosensors to be switched to fluorescence intensity, lifetime or bioluminescence. These FRET pairs thus establish a new concept for the development of highly sensitive and tunable biosensors.

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Competing Interest Statement

K.J. is listed as inventor for patents related to labeling technologies filed by the Max Planck Society or the Ecole Polytechnique Federale de Lausanne (EPFL).

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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 4.0 International license.
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Posted November 29, 2022.
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A general method for the development of multicolor biosensors with large dynamic ranges
Lars Hellweg, Anna Edenhofer, Lucas Barck, Magnus-Carsten Huppertz, Michelle. S. Frei, Miroslaw Tarnawski, Andrea Bergner, Birgit Koch, Kai Johnsson, Julien Hiblot
bioRxiv 2022.11.29.518186; doi: https://doi.org/10.1101/2022.11.29.518186
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A general method for the development of multicolor biosensors with large dynamic ranges
Lars Hellweg, Anna Edenhofer, Lucas Barck, Magnus-Carsten Huppertz, Michelle. S. Frei, Miroslaw Tarnawski, Andrea Bergner, Birgit Koch, Kai Johnsson, Julien Hiblot
bioRxiv 2022.11.29.518186; doi: https://doi.org/10.1101/2022.11.29.518186

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