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Fluorescence lifetime enables high-resolution analysis of neuromodulator dynamics across time and animals

View ORCID ProfilePingchuan Ma, Peter Chen, Elizabeth Tilden, Samarth Aggarwal, Anna Oldenborg, Yao Chen
doi: https://doi.org/10.1101/2022.09.28.510014
Pingchuan Ma
1Department of Neuroscience, Washington University in St. Louis, St. Louis, MO 63110
2Ph.D. Program in Neuroscience, Washington University in St. Louis
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  • ORCID record for Pingchuan Ma
Peter Chen
1Department of Neuroscience, Washington University in St. Louis, St. Louis, MO 63110
3Master’s Program in Biomedical Engineering, Washington University in St. Louis
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Elizabeth Tilden
1Department of Neuroscience, Washington University in St. Louis, St. Louis, MO 63110
2Ph.D. Program in Neuroscience, Washington University in St. Louis
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Samarth Aggarwal
1Department of Neuroscience, Washington University in St. Louis, St. Louis, MO 63110
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Anna Oldenborg
1Department of Neuroscience, Washington University in St. Louis, St. Louis, MO 63110
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Yao Chen
1Department of Neuroscience, Washington University in St. Louis, St. Louis, MO 63110
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  • For correspondence: yaochen@wustl.edu
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ABSTRACT

Optical sensors have transformed the field of neuromodulation because neuromodulator dynamics are essential for their function. Despite their high spatial and temporal resolution, these fluorescence intensity-based sensors are sensitive to sensor expression level and excitation light fluctuation, thus preventing analysis of neuromodulators across time or animals. Here, we screened neuromodulator sensors and discovered that multiple sensors showed response in fluorescence lifetime, a property independent of sensor expression or excitation light power. The acetylcholine sensor GRAB-ACh3.0 showed the largest lifetime change. Fluorescence lifetime of GRAB-ACh3.0 responds to transient ACh release, is dose sensitive, and is insensitive to excitation laser power. In mice across sleep/wake and running/resting states, fluorescence lifetime, in contrast to intensity, predicts behavior states accurately despite change in sensor expression level across weeks and animals. Thus, fluorescence lifetime of neuromodulator sensors enables comparison of neuromodulator dynamics at high resolution across different animals, brain regions, disease models, and chronic time scales.

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-ND 4.0 International license.
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Posted September 30, 2022.
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Fluorescence lifetime enables high-resolution analysis of neuromodulator dynamics across time and animals
Pingchuan Ma, Peter Chen, Elizabeth Tilden, Samarth Aggarwal, Anna Oldenborg, Yao Chen
bioRxiv 2022.09.28.510014; doi: https://doi.org/10.1101/2022.09.28.510014
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Fluorescence lifetime enables high-resolution analysis of neuromodulator dynamics across time and animals
Pingchuan Ma, Peter Chen, Elizabeth Tilden, Samarth Aggarwal, Anna Oldenborg, Yao Chen
bioRxiv 2022.09.28.510014; doi: https://doi.org/10.1101/2022.09.28.510014

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