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. 2024 Jun 3.
doi: 10.1007/s12264-024-01235-w. Online ahead of print.

Development and Application of a Mitochondrial Genetically Encoded Voltage Indicator in Narcosis

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Development and Application of a Mitochondrial Genetically Encoded Voltage Indicator in Narcosis

Run-Zhou Yang et al. Neurosci Bull. .

Abstract

Mitochondrial membrane potential (MMP) plays a crucial role in the function of cells and organelles, involving various cellular physiological processes, including energy production, formation of reactive oxygen species (ROS), unfolded protein stress, and cell survival. Currently, there is a lack of genetically encoded fluorescence indicators (GEVIs) for MMP. In our screening of various GEVIs for their potential monitoring MMP, the Accelerated Sensor of Action Potentials (ASAP) demonstrated optimal performance in targeting mitochondria and sensitivity to depolarization in multiple cell types. However, mitochondrial ASAPs also displayed sensitivity to ROS in cardiomyocytes. Therefore, two ASAP mutants resistant to ROS were generated. A double mutant ASAP3-ST exhibited the highest voltage sensitivity but weaker fluorescence. Overall, four GEVIs capable of targeting mitochondria were obtained and named mitochondrial potential indicators 1-4 (MPI-1-4). In vivo, fiber photometry experiments utilizing MPI-2 revealed a mitochondrial depolarization during isoflurane-induced narcosis in the M2 cortex.

Keywords: Fiber photometry; Genetically encoded voltage indicators; Isoflurane-induced narcosis; M2 cortex; Membrane potential; Mitochondria; ROS sensitivity.

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References

    1. Vyas S, Zaganjor E, Haigis MC. Mitochondria and cancer. Cell 2016, 166: 555–566. - DOI - PubMed - PMC
    1. Zorova LD, Popkov VA, Plotnikov EY, Silachev DN, Pevzner IB, Jankauskas SS. Mitochondrial membrane potential. Anal Biochem 2018, 552: 50–59. - DOI - PubMed
    1. O’Rourke B, Cortassa S, Aon MA. Mitochondrial ion channels: Gatekeepers of life and death. Physiology 2005, 20: 303–315. - DOI - PubMed
    1. Dzbek J, Korzeniewski B. Control over the contribution of the mitochondrial membrane potential (ΔΨ) and proton gradient (ΔpH) to the protonmotive force (Δp). In silico studies. J Biol Chem 2008, 283: 33232–33239. - DOI - PubMed - PMC
    1. Huang S, Ratliff KS, Matouschek A. Protein unfolding by the mitochondrial membrane potential. Nat Struct Biol 2002, 9: 301–307. - DOI - PubMed

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