4.8 Article

Archaerhodopsin variants with enhanced voltage-sensitive fluorescence in mammalian and Caenorhabditis elegans neurons

Journal

NATURE COMMUNICATIONS
Volume 5, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms5894

Keywords

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Funding

  1. NIH/NINDS New Innovator [NIH IDP20D017782-01]
  2. President and Provost of California Institute of Technology
  3. Biology and Biological Engineering Division of California Institute of Technology
  4. Beckman Institute of Caltech
  5. Gordon and Betty Moore Foundation [GBMF2809]
  6. NIH [1R21MH103824-01, 1R01NS085910-01, 1R01AG047664-01]
  7. Institute for Collaborative Biotechnologies through grant from the U.S. Army Research Office [W911NF-09-0001]
  8. Human Frontiers in Science Program
  9. Mallinckrodt Foundation
  10. Pew Charitable Trust
  11. Michael J. Fox Foundation
  12. Kimmel Foundation
  13. Caltech-GIST
  14. HHMI
  15. Caltech Biology Division Training grant [NIH/NRSA 5T32GM07616]
  16. German Research Foundation (DFG) [EN 957/1-1]

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Probing the neural circuit dynamics underlying behaviour would benefit greatly from improved genetically encoded voltage indicators. The proton pump Archaerhodopsin-3 (Arch), an optogenetic tool commonly used for neuronal inhibition, has been shown to emit voltage-sensitive fluorescence. Here we report two Arch variants with enhanced radiance (Archers) that in response to 655 nm light have 3-5 times increased fluorescence and 55-99 times reduced photocurrents compared with Arch WT. The most fluorescent variant, Archer1, has 25-40% fluorescence change in response to action potentials while using 9 times lower light intensity compared with other Arch-based voltage sensors. Archer1 is capable of wavelength-specific functionality as a voltage sensor under red light and as an inhibitory actuator under green light. As a proof-of-concept for the application of Arch-based sensors in vivo, we show fluorescence voltage sensing in behaving Caenorhabditis elegans. Archer1's characteristics contribute to the goal of all-optical detection and modulation of activity in neuronal networks in vivo.

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