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Absolute measurement of cellular activities using photochromic single-fluorophore biosensors and intermittent quantification

Author

Listed:
  • Franziska Bierbuesse

    (KU Leuven)

  • Anaïs C. Bourges

    (KU Leuven)

  • Vincent Gielen

    (KU Leuven)

  • Viola Mönkemöller

    (KU Leuven)

  • Wim Vandenberg

    (KU Leuven)

  • Yi Shen

    (University of Alberta)

  • Johan Hofkens

    (KU Leuven)

  • Pieter Vanden Berghe

    (KU Leuven)

  • Robert E. Campbell

    (University of Alberta
    University of Tokyo)

  • Benjamien Moeyaert

    (KU Leuven)

  • Peter Dedecker

    (KU Leuven)

Abstract

Genetically-encoded biosensors based on a single fluorescent protein are widely used to visualize analyte levels or enzymatic activities in cells, though usually to monitor relative changes rather than absolute values. We report photochromism-enabled absolute quantification (PEAQ) biosensing, a method that leverages the photochromic properties of biosensors to provide an absolute measure of the analyte concentration or activity. We develop proof-of-concept photochromic variants of the popular GCaMP family of Ca2+ biosensors, and show that these can be used to resolve dynamic changes in the absolute Ca2+ concentration in live cells. We also develop intermittent quantification, a technique that combines absolute aquisitions with fast fluorescence acquisitions to deliver fast but fully quantitative measurements. We also show how the photochromism-based measurements can be expanded to situations where the absolute illumination intensities are unknown. In principle, PEAQ biosensing can be applied to other biosensors with photochromic properties, thereby expanding the possibilities for fully quantitative measurements in complex and dynamic systems.

Suggested Citation

  • Franziska Bierbuesse & Anaïs C. Bourges & Vincent Gielen & Viola Mönkemöller & Wim Vandenberg & Yi Shen & Johan Hofkens & Pieter Vanden Berghe & Robert E. Campbell & Benjamien Moeyaert & Peter Dedecke, 2022. "Absolute measurement of cellular activities using photochromic single-fluorophore biosensors and intermittent quantification," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-29508-w
    DOI: 10.1038/s41467-022-29508-w
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    References listed on IDEAS

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    1. Benjamien Moeyaert & Graham Holt & Rajtarun Madangopal & Alberto Perez-Alvarez & Brenna C. Fearey & Nicholas F. Trojanowski & Julia Ledderose & Timothy A. Zolnik & Aniruddha Das & Davina Patel & Timot, 2018. "Improved methods for marking active neuron populations," Nature Communications, Nature, vol. 9(1), pages 1-12, December.
    2. Namrata Ojha & Kristin H. Rainey & George H. Patterson, 2020. "Imaging of fluorescence anisotropy during photoswitching provides a simple readout for protein self-association," Nature Communications, Nature, vol. 11(1), pages 1-11, December.
    3. Tsai-Wen Chen & Trevor J. Wardill & Yi Sun & Stefan R. Pulver & Sabine L. Renninger & Amy Baohan & Eric R. Schreiter & Rex A. Kerr & Michael B. Orger & Vivek Jayaraman & Loren L. Looger & Karel Svobod, 2013. "Ultrasensitive fluorescent proteins for imaging neuronal activity," Nature, Nature, vol. 499(7458), pages 295-300, July.
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