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Removing direct photocurrent artifacts in optogenetic connectivity mapping data via constrained matrix factorization

View ORCID ProfileBenjamin Antin, View ORCID ProfileMasato Sadahiro, View ORCID ProfileMarta Gajowa, View ORCID ProfileMarcus A. Triplett, View ORCID ProfileHillel Adesnik, View ORCID ProfileLiam Paninski
doi: https://doi.org/10.1101/2023.07.13.548849
Benjamin Antin
1Mortimer B. Zuckerman Mind Brain Behavior Institute, Columbia University, NY
2Grossman Center for the Statistics of Mind, Columbia University, NY
3Center for Theoretical Neuroscience, Columbia University, NY
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  • ORCID record for Benjamin Antin
  • For correspondence: ba2617@cumc.columbia.edu
Masato Sadahiro
5Department of Molecular and Cell Biology, University of California, Berkeley, CA
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  • For correspondence: ba2617@cumc.columbia.edu
Marta Gajowa
5Department of Molecular and Cell Biology, University of California, Berkeley, CA
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  • ORCID record for Marta Gajowa
Marcus A. Triplett
1Mortimer B. Zuckerman Mind Brain Behavior Institute, Columbia University, NY
2Grossman Center for the Statistics of Mind, Columbia University, NY
3Center for Theoretical Neuroscience, Columbia University, NY
4Department of Statistics, Columbia University, NY
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Hillel Adesnik
5Department of Molecular and Cell Biology, University of California, Berkeley, CA
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Liam Paninski
1Mortimer B. Zuckerman Mind Brain Behavior Institute, Columbia University, NY
2Grossman Center for the Statistics of Mind, Columbia University, NY
3Center for Theoretical Neuroscience, Columbia University, NY
4Department of Statistics, Columbia University, NY
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Abstract

Monosynaptic connectivity mapping is crucial for building circuit-level models of neural computation. Two-photon optogenetic stimulation, when combined with whole-cell recordings, has the potential to map monosynaptic connectivity at an unprecedented scale. However, optogenetic mapping of nearby connections poses a challenge, due to stimulation artifacts. When the postsynaptic cell expresses opsin, optical excitation can directly induce current in the patched cell, confounding connectivity measurements. This problem is most severe in nearby cell pairs, where synaptic connectivity is often strongest. To overcome this problem, we developed a computational tool, Photocurrent Removal with Constraints (PhoRC). Our method is based on a constrained matrix factorization model which leverages the fact that photocurrent kinetics are consistent across repeated stimulations at similar laser power. We demonstrate on real and simulated data that PhoRC consistently removes photocurrents while preserving synaptic currents, despite variations in photocurrent kinetics across datasets. Our method allows the discovery of synaptic connections which would have been otherwise obscured by photocurrent artifacts, and may thus reveal a more complete picture of synaptic connectivity. PhoRC runs faster than real time and is available at https://github.com/bantin/PhoRC.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://github.com/bantin/PhoRC

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted July 15, 2023.
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Removing direct photocurrent artifacts in optogenetic connectivity mapping data via constrained matrix factorization
Benjamin Antin, Masato Sadahiro, Marta Gajowa, Marcus A. Triplett, Hillel Adesnik, Liam Paninski
bioRxiv 2023.07.13.548849; doi: https://doi.org/10.1101/2023.07.13.548849
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Removing direct photocurrent artifacts in optogenetic connectivity mapping data via constrained matrix factorization
Benjamin Antin, Masato Sadahiro, Marta Gajowa, Marcus A. Triplett, Hillel Adesnik, Liam Paninski
bioRxiv 2023.07.13.548849; doi: https://doi.org/10.1101/2023.07.13.548849

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