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A modular chemigenetic calcium indicator for multiplexed in vivo functional imaging

  • Helen Farrants,
  • Yichun Shuai,
  • William C. Lemon,
  • Christian Monroy Hernandez,
  • Deng Zhang,
  • Shang Yang,
  • Ronak Patel,
  • Guanda Qiao,
  • Michelle S. Frei,
  • Sarah E. Plutkis,
  • Jonathan B. Grimm,
  • Timothy L. Hanson,
  • Filip Tomaska,
  • Glenn C. Turner,
  • Carsen Stringer,
  • Philipp J. Keller,
  • Abraham G. Beyene,
  • Yao Chen,
  • Yajie Liang,
  • Luke D. Lavis,
  • Eric R. Schreiter

摘要

Genetically encoded fluorescent calcium indicators allow cellular-resolution recording of physiology. However, bright, genetically targetable indicators that can be multiplexed with existing tools in vivo are needed for simultaneous imaging of multiple signals. Here we describe WHaloCaMP, a modular chemigenetic calcium indicator built from bright dye-ligands and protein sensor domains. Fluorescence change in WHaloCaMP results from reversible quenching of the bound dye via a strategically placed tryptophan. WHaloCaMP is compatible with rhodamine dye-ligands that fluoresce from green to near-infrared, including several that efficiently label the brain in animals. When bound to a near-infrared dye-ligand, WHaloCaMP shows a 7× increase in fluorescence intensity and a 2.1-ns increase in fluorescence lifetime upon calcium binding. We use WHaloCaMP1a to image Ca2+ responses in vivo in flies and mice, to perform three-color multiplexed functional imaging of hundreds of neurons and astrocytes in zebrafish larvae and to quantify Ca2+ concentration using fluorescence lifetime imaging microscopy (FLIM).