A luminescent calcium biosensor enabling endpoint measurement of GPCR-mediated calcium signaling

G<sub>q/11</sub>-coupled GPCRs regulate critical physiological processes through calcium mobilization, making intracellular Ca<sup>2+</sup> dynamics a key readout for drug discovery and biomarker detection. However, the transient nature of calcium signals necessitates real-time monitoring with specialized equipment, creating barriers for high-throughput screening and limiting accessibility. Here we present CalLuc-2.1, a luminescent calcium biosensor that converts brief Ca<sup>2+</sup> spikes into persistent luminescence changes readable tens of minutes after stimulation. By eliminating the need for precisely-timed detection, CalLuc-2.1 enables endpoint measurement of GPCR activation using standard plate readers. We demonstrate robust performance (Z' > 0.88) across multiple G<sub>q/11</sub>-coupled GPCRs in both agonist and antagonist screening formats. Furthermore, CalLuc-2.1 successfully detects endogenous GPCR ligands directly in human serum, offering a simpler alternative to immunoassays and mass spectrometry for biomarker quantification. This approach makes calcium-based GPCR assays accessible to any laboratory with basic luminescence detection capabilities, potentially accelerating both drug discovery and clinical research applications.

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Publication Details

Journal
Communications Biology
Published
2026-03-29
DOI
https://doi.org/10.1038/s42003-026-09920-4
Primary Topic
Receptor Mechanisms and Signaling
Type
article
Field-Weighted Citation Impact
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article

A luminescent calcium biosensor enabling endpoint measurement of GPCR-mediated calcium signaling

Ryoji Kise, Masataka Yanagawa, Kosuke Doi, Kota Shimizume et al.
Communications Biology
Receptor Mechanisms and Signaling
article

A luminescent calcium biosensor enabling endpoint measurement of GPCR-mediated calcium signaling

Ryoji Kise, Masataka Yanagawa, Kosuke Doi, Kota Shimizume, Asuka Inoue
article en

Abstract

G<sub>q/11</sub>-coupled GPCRs regulate critical physiological processes through calcium mobilization, making intracellular Ca<sup>2+</sup> dynamics a key readout for drug discovery and biomarker detection. However, the transient nature of calcium signals necessitates real-time monitoring with specialized equipment, creating barriers for high-throughput screening and limiting accessibility. Here we present CalLuc-2.1, a luminescent calcium biosensor that converts brief Ca<sup>2+</sup> spikes into persistent luminescence changes readable tens of minutes after stimulation. By eliminating the need for precisely-timed detection, CalLuc-2.1 enables endpoint measurement of GPCR activation using standard plate readers. We demonstrate robust performance (Z' > 0.88) across multiple G<sub>q/11</sub>-coupled GPCRs in both agonist and antagonist screening formats. Furthermore, CalLuc-2.1 successfully detects endogenous GPCR ligands directly in human serum, offering a simpler alternative to immunoassays and mass spectrometry for biomarker quantification. This approach makes calcium-based GPCR assays accessible to any laboratory with basic luminescence detection capabilities, potentially accelerating both drug discovery and clinical research applications.

Communications Biology
Pioneer (United States) (US), Tohoku University (JP), Kyoto University (JP), Kyoto Pharmaceutical University (JP), Yamasa Corporation (Japan) (JP), Tohoku Medical and Pharmaceutical University (JP)
Affordable and clean energy
Openalex Percentile: Top 4%
Receptor Mechanisms and Signaling
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A luminescent calcium biosensor enabling endpoint measurement of GPCR-mediated calcium signaling — Ryoji Kise, Masataka Yanagawa, et al. · Communications Biology (2026) | TGRS Research Map | TGRS