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A near-infrared genetically encoded calcium indicator for in vivo imaging

  • Anton A. Shemetov
  • , Mikhail V. Monakhov
  • , Qinrong Zhang
  • , Jose Ernesto Canton-Josh
  • , Manish Kumar
  • , Maomao Chen
  • , Mikhail E. Matlashov
  • , Xuan Li
  • , Wei Yang
  • , Liming Nie
  • , Daria M. Shcherbakova
  • , Yevgenia Kozorovitskiy
  • , Junjie Yao
  • , Na Ji
  • , Vladislav V. Verkhusha*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

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 languageEnglish
Pages (from-to)368-377
JournalNature Biotechnology
Volume39
Issue number3
Online published26 Oct 2020
DOIs
Publication statusPublished - Mar 2021
Externally publishedYes

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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