4.8 Article

Ultrafast Two-Photon Imaging of a High-Gain Voltage Indicator in Awake Behaving Mice

期刊

CELL
卷 179, 期 7, 页码 1590-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2019.11.004

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资金

  1. NIH BRAIN Initiative [1U01NS090600, 1U01NS103464, 1RF1MH11410501]
  2. La Fondation pour la Recherche Medicale grant Equipes [FRM DEQ20140329498]
  3. Agence Nationale de la Recherche [ALPINS ANR-15-CE19-0011, ANR-10-LABX-54 MEMO LIFE, ANR-11-IDEX-0001-02 PSL*, ANR-10-INSB-04-01]
  4. Canadian Institutes of Health Research [MOP-81142]
  5. Natural Sciences and Engineering Research Council of Canada [RGPIN-2015-06266]
  6. National Natural Science Foundation of China [31630030]
  7. NSF NeuroNex Technology Hub award [1707261]
  8. Marc A. Cohen Graduate Fellowship Research Fund
  9. Stanford Bioengineering PhD Program
  10. American Epilepsy Society predoctoral fellowship
  11. China Scholarship Council
  12. Stanford Neuroscience PhD Program training grant [5T32MH020016]
  13. Natural Sciences and Engineering Research Council of Canada
  14. CNRS
  15. Ecole Normale Superieure
  16. NIH [P30NS069375]
  17. NERF [2009-44, 2011-45]
  18. Fondation pour la Recherche Medicale [DGE 20111123023]
  19. Federation pour la Recherche sur le Cerveau
  20. Rotary International France
  21. Post-9/11 GI Bill
  22. INSERM

向作者/读者索取更多资源

Optical interrogation of voltage in deep brain locations with cellular resolution would be immensely useful for understanding how neuronal circuits process information. Here, we report ASAP3, a genetically encoded voltage indicator with 51% fluorescence modulation by physiological voltages, submillisecond activation kinetics, and full responsivity under two-photon excitation. We also introduce an ultrafast local volume excitation (ULoVE) method for kilohertz-rate two-photon sampling in vivo with increased stability and sensitivity. Combining a soma-targeted ASAP3 variant and ULoVE, we show single-trial tracking of spikes and subthreshold events for minutes in deep locations, with subcellular resolution and with repeated sampling over days. In the visual cortex, we use soma-targeted ASAP3 to illustrate cell-type-dependent subthreshold modulation by locomotion. Thus, ASAP3 and ULoVE enable high-speed optical recording of electrical activity in genetically defined neurons at deep locations during awake behavior.

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