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Key Organism Strain Cell Line Gene Symbol Protein name Protein tag Reporter Project ID Dataset ID Title Description Data Type Gene Ontology Biological Imaging Methods Method Summary Paper Information Medical Subject Headlines Person

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476-Matsuda-GreenRedFRET

https://ssbd.riken.jp/database/476-Matsuda-GreenRedFRET/

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ssbd-repos-000476

https://ssbd.riken.jp/repository/476/

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Calcium imaging of HeLa cells in response to histamine using improved Green-Red FRET sensors

To monitor the calcium dynamics in cells, various genetically encoded calcium indicators (GECIs) based on FRET between fluorescent proteins are widely used for live imaging. Conventionally, cyan and yellow fluorescent proteins have been often used as FRET pairs. Meanwhile, bathochromically shifted indicators with green and red fluorescent protein pairs have various advantages, such as low toxicity and autofluorescence in cells. However, it remains difficult to develop them with a similar level of dynamic range as cyan and yellow fluorescent protein pairs. To improve this, we used Gamillus, which has a unique trans-configuration chromophore, as a green fluorescent protein. Based on one of the best high-dynamic-range GECIs, Twitch-NR, the authors developed a GECI with 1.5-times higher dynamic range, Twitch-GmRR, using RRvT as a red fluorescent protein. Twitch-GmRR had high brightness and photostability and was successfully applied for imaging the calcium dynamics in live cells. Our results suggest that Gamillus with trans-type chromophores contributes to improving the dynamic range of GECIs. Therefore, selection of the cis-trans isomer of the chromophore may be a fundamental approach to improve the dynamic range of green-red FRET indicators, unlimited by GECIs.

2026-06-09

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CC BY 4.0

Image data based on Experiment

2 ( Image datasets: 2, Quantitative data datasets: 0 )

610.6 MB ( Image datasets: 610.6 MB, Quantitative data datasets: 0 bytes )

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Homo sapiens

HeLa Cell

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response to histamine calcium ion import into cytosol

cytosol

spinning disk confocal microscopy

3 seconds

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Tomoki Matsuda, Takeharu Nagai , Kitasato University, Osaka University , School of Science, SANKEN , School of Science, SANKEN

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