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Updated: Sep 8, 2025

In Vivo Functional Brain Imaging Approach Based on Bioluminescent Calcium Indicator GFP-aequorin
Published on: January 8, 2016
An Enhanced Red Bioluminescent Indicator for Responsive Detection of Physiological Calcium Dynamics in Cells and Mice
Xiaodong Tian1,2, Yiyu Zhang1,2, Haoyang Du3
1Department of Molecular Physiology and Biological Physics, University of Virginia School of Medicine, Charlottesville, Virginia 22908, United States.
Abstract:
Calcium (Ca2+) is a crucial metal ion and signaling messenger. While bioluminescent indicators for Ca2+ have emerged as powerful imaging tools, their performance has been suboptimal. In this study, we developed an enhanced bioluminescent red indicator for Ca2+ (eBRIC) by using a physiological Ca2+ concentration range during library screening. Compared with its predecessors, this new sensor demonstrates substantially improved Ca2+ responsiveness in protein-based assays, cultured cell lines, and primary neurons. We further demonstrated the utility of eBRIC for the in vivo recording of Ca2+ dynamics in the brains of live mice, using both a microscope setup and a luminescent imaging dark box. Notably, by combining eBRIC with our recently developed water-soluble luciferin, we achieved minimally invasive, video-rate imaging of Ca2+ activity in a defined brain region of awake mice. In a footshock-induced basolateral amygdala activation paradigm, eBRIC elicited approximately double the response compared to the previous BRIC indicator. The improved responsiveness offered by eBRIC underscores its potential as a powerful tool for investigating Ca2+ dynamics in living systems.

