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suck abstract from ncbi


10.1038/s42003-021-01916-6

http://scihub22266oqcxt.onion/10.1038/s42003-021-01916-6
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33758369!7988155!33758369
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suck abstract from ncbi

pmid33758369      Commun+Biol 2021 ; 4 (1): 389
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  • Imaging the electrical activity of organelles in living cells #MMPMID33758369
  • Matamala E; Castillo C; Vivar JP; Rojas PA; Brauchi SE
  • Commun Biol 2021[Mar]; 4 (1): 389 PMID33758369show ga
  • Eukaryotic cells are complex systems compartmentalized in membrane-bound organelles. Visualization of organellar electrical activity in living cells requires both a suitable reporter and non-invasive imaging at high spatiotemporal resolution. Here we present hVoS(org), an optical method to monitor changes in the membrane potential of subcellular membranes. This method takes advantage of a FRET pair consisting of a membrane-bound voltage-insensitive fluorescent donor and a non-fluorescent voltage-dependent acceptor that rapidly moves across the membrane in response to changes in polarity. Compared to the currently available techniques, hVoS(org) has advantages including simple and precise subcellular targeting, the ability to record from individual organelles, and the potential for optical multiplexing of organellar activity.
  • |*Biosensing Techniques[MESH]
  • |*Membrane Potentials[MESH]
  • |*Microscopy, Fluorescence[MESH]
  • |*Optical Imaging[MESH]
  • |Animals[MESH]
  • |Endoplasmic Reticulum/metabolism/*physiology[MESH]
  • |Fluorescence Resonance Energy Transfer[MESH]
  • |Genes, Reporter[MESH]
  • |Golgi Apparatus/metabolism/*physiology[MESH]
  • |HEK293 Cells[MESH]
  • |Humans[MESH]
  • |Luminescent Proteins/genetics/metabolism[MESH]
  • |MCF-7 Cells[MESH]
  • |Optogenetics[MESH]
  • |PC12 Cells[MESH]


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