Bioluminescent Low-Affinity Ca2+ Indicator for ER with Multicolor Calcium Imaging in Single Living Cells

ACS Chem Biol. 2018 Jul 20;13(7):1862-1871. doi: 10.1021/acschembio.7b01014. Epub 2018 Mar 9.

Abstract

The sarco/endoplasmic reticulum (SR/ER) is the foremost intercellular Ca2+ store (at submillimolar concentrations), playing a crucial role in controlling intracellular Ca2+ levels. For the investigation of SR/ER Ca2+ dynamics in cells, fluorescent protein-based genetically encoded calcium indicators (GECIs) with low Ca2+ affinity have been used. Recently, bioluminescent protein-based GECIs with high brightness have been reported to counter the constraints of fluorescence imaging, such as phototoxicity. However, their Ca2+ affinity is high and limited for imaging in the cytosol, nucleus, or mitochondria. In this study, we developed a novel cyan color, low-affinity ( Kd = 110 μM) intensiometric bioluminescent GECI, which enables monitoring of the Ca2+ dynamics in the ER of HeLa cells and the SR of C2C12-derived myotubes. To facilitate the broad concentration range of Ca2+ in cellular organelles, we additionally developed an intermediate affinity ( Kd = 18 μM), orange color, and bioluminescent GECI, which enables monitoring of Ca2+ dynamics in the mitochondria of HeLa cells. With these indicators, in conjunction with an existing high-affinity, green, bioluminescent GECI, we succeeded in multicolor bioluminescent Ca2+ imaging in three distinct organelles (nuclei, mitochondria, and ER) simultaneously. The multicolor, live, bioluminescent Ca2+ imaging demonstrated here can be used to stably reveal the ER Ca2+ homeostasis and cooperative Ca2+ regulation among organelles. This will lead to the further understanding of Ca2+-related physiological functions and pathophysiological mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Cell Nucleus / metabolism
  • Color
  • Endoplasmic Reticulum / metabolism*
  • Fluorescence
  • Fluorescent Dyes / chemistry*
  • HeLa Cells
  • Humans
  • Luminescent Proteins / chemistry*
  • Luminescent Proteins / genetics
  • Mice
  • Microscopy, Fluorescence / methods
  • Mitochondria / metabolism
  • Muscle Fibers, Skeletal / metabolism
  • Mutation
  • Sarcoplasmic Reticulum / metabolism

Substances

  • Fluorescent Dyes
  • Luminescent Proteins
  • Calcium