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Genetically encoded bioluminescent voltage indicator for multi-purpose use in wide range of bioimaging.


ABSTRACT: We report development of the first genetically encoded bioluminescent indicator for membrane voltage called LOTUS-V. Since it is bioluminescent, imaging LOTUS-V does not require external light illumination. This allows bidirectional optogenetic control of cellular activity triggered by Channelrhodopsin2 and Halorhodopsin during voltage imaging. The other advantage of LOTUS-V is the robustness of a signal-to-background ratio (SBR) wherever it expressed, even in the specimens where autofluorescence from environment severely interferes fluorescence imaging. Through imaging of moving cardiomyocyte aggregates, we demonstrated the advantages of LOTUS-V in long-term imaging are attributable to the absence of phototoxicity, and photobleaching in bioluminescent imaging, combined with the ratiometric aspect of LOTUS-V design. Collectively LOTUS-V extends the scope of excitable cell control and simultaneous voltage phenotyping, which should enable applications in bioscience, medicine and pharmacology previously not possible.

SUBMITTER: Inagaki S 

PROVIDER: S-EPMC5322354 | biostudies-literature | 2017 Feb

REPOSITORIES: biostudies-literature

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Genetically encoded bioluminescent voltage indicator for multi-purpose use in wide range of bioimaging.

Inagaki Shigenori S   Tsutsui Hidekazu H   Suzuki Kazushi K   Agetsuma Masakazu M   Arai Yoshiyuki Y   Jinno Yuka Y   Bai Guirong G   Daniels Matthew J MJ   Okamura Yasushi Y   Matsuda Tomoki T   Nagai Takeharu T  

Scientific reports 20170213


We report development of the first genetically encoded bioluminescent indicator for membrane voltage called LOTUS-V. Since it is bioluminescent, imaging LOTUS-V does not require external light illumination. This allows bidirectional optogenetic control of cellular activity triggered by Channelrhodopsin2 and Halorhodopsin during voltage imaging. The other advantage of LOTUS-V is the robustness of a signal-to-background ratio (SBR) wherever it expressed, even in the specimens where autofluorescenc  ...[more]

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