4.8 Article

A photoswitchable GPCR-based opsin for presynaptic inhibition

Journal

NEURON
Volume 109, Issue 11, Pages 1791-+

Publisher

CELL PRESS
DOI: 10.1016/j.neuron.2021.04.026

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Funding

  1. NIH BRAIN Initiative [R01 MH111520]
  2. NIH [R21 DA049569, K01 DA042219, K01 DK115634, T32DA007278, R35 GM122577, P30DA048736]
  3. Mary Gates Research Fellowship
  4. Scan Design Research Foundation
  5. Hope Center Viral Vectors Core at Washington University School of Medicine

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This study introduces a GPCR-based opsin called parapinopsin (PPO), which can rapidly and reversibly inhibit the release of glutamate, GABA, and dopamine at presynaptic terminals by coupling with G(i/o) signaling cascades. PPO alters reward behaviors in a time-locked and reversible manner in vivo, filling a significant gap in the neuroscience toolkit for rapid and reversible synaptic inhibition.
Optical manipulations of genetically defined cell types have generated significant insights into the dynamics of neural circuits. While optogenetic activation has been relatively straightforward, rapid and reversible synaptic inhibition has proven more elusive. Here, we leveraged the natural ability of inhibitory presynaptic GPCRs to suppress synaptic transmission and characterize parapinopsin (PPO) as a GPCR-based opsin for terminal inhibition. PPO is a photoswitchable opsin that couples to G(i/o) signaling cascades and is rapidly activated by pulsed blue light, switched off with amber light, and effective for repeated, prolonged, and reversible inhibition. PPO rapidly and reversibly inhibits glutamate, GABA, and dopamine release at presynaptic terminals. Furthermore, PPO alters reward behaviors in a time-locked and reversible manner in vivo. These results demonstrate that PPO fills a significant gap in the neuroscience toolkit for rapid and reversible synaptic inhibition and has broad utility for spatiotemporal control of inhibitory GPCR signaling cascades.

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