Abstract
While calcium imaging has become a mainstay of modern neuroscience, the spectral properties of current fluorescent calcium indicators limit deep-tissue imaging as well as simultaneous use with other probes. Using two monomeric near-infrared (NIR) fluorescent proteins (FPs), we engineered an NIR Förster resonance energy transfer (FRET)-based genetically encoded calcium indicator (iGECI). iGECI exhibits high levels of brightness and photostability and an increase up to 600% in the fluorescence response to calcium. In dissociated neurons, iGECI detects spontaneous neuronal activity and electrically and optogenetically induced firing. We validated the performance of iGECI up to a depth of almost 400 µm in acute brain slices using one-photon light-sheet imaging. Applying hybrid photoacoustic and fluorescence microscopy, we simultaneously monitored neuronal and hemodynamic activities in the mouse brain through an intact skull, with resolutions of ~3 μm (lateral) and ~25–50 μm (axial). Using two-photon imaging, we detected evoked and spontaneous neuronal activity in the mouse visual cortex, with fluorescence changes of up to 25%. iGECI allows biosensors and optogenetic actuators to be multiplexed without spectral crosstalk. © 2020, The Author(s), under exclusive licence to Springer Nature America, Inc.
| Original language | English |
|---|---|
| Pages (from-to) | 368-377 |
| Journal | Nature Biotechnology |
| Volume | 39 |
| Issue number | 3 |
| Online published | 26 Oct 2020 |
| DOIs | |
| Publication status | Published - Mar 2021 |
| Externally published | Yes |
Funding
This work was supported by grants GM122567, NS103573, NS115581 (all to V.V.V.), EY030705 (to D.M.S.), EB028143, NS111039, EB027304, CA243822 (all to J.Y.) and MH117111 and NS107539 (both to Y.K.) from the National Institutes of Health; 18CSA34080277 from the American Heart Association (to J.Y.); a Beckman Young Investigator Award, a Searle Scholar Award and a Rita Allen Foundation Award (all to Y.K). J.E.C.-J. is a T32 NS041234 fellow.
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