4.8 Article

A calibrated optogenetic toolbox of stable zebrafish opsin lines

Journal

ELIFE
Volume 9, Issue -, Pages -

Publisher

ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.54937

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Funding

  1. Horizon 2020 Framework Programme Marie Curie Incoming International Fellowship, H2020-MSCA-IF-2016 Project [752199]
  2. Human Frontier Science Program [RGP063-2018, LT393/2010]
  3. New York Stem Cell Foundation [NYSCF-R-NI39]
  4. Wellcome [204708/Z/16/Z, 101195/Z/13/Z]
  5. Royal Society [101195/Z/13/Z]
  6. University College London
  7. Deutsche Forschungsgemeinschaft [SPP1926]
  8. Max Planck Society
  9. Agence Nationale de la Recherche [ANR-10-IAIHU-06, ANR-11-INBS-0011]
  10. Wellcome Trust [101195/Z/13/Z, 204708/Z/16/Z] Funding Source: Wellcome Trust
  11. Marie Curie Actions (MSCA) [752199] Funding Source: Marie Curie Actions (MSCA)

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Optogenetic actuators with diverse spectral tuning, ion selectivity and kinetics are constantly being engineered providing powerful tools for controlling neural activity with subcellular resolution and millisecond precision. Achieving reliable and interpretable in vivo optogenetic manipulations requires reproducible actuator expression and calibration of photocurrents in target neurons. Here, we developed nine transgenic zebrafish lines for stable opsin expression and calibrated their efficacy in vivo. We first used high-throughput behavioural assays to compare opsin ability to elicit or silence neural activity. Next, we performed in vivo whole-cell electrophysiological recordings to quantify the amplitude and kinetics of photocurrents and test opsin ability to precisely control spiking. We observed substantial variation in efficacy, associated with differences in both opsin expression level and photocurrent characteristics, and identified conditions for optimal use of the most efficient opsins. Overall, our calibrated optogenetic toolkit will facilitate the design of controlled optogenetic circuit manipulations.

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