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Tytuł pozycji:

Measuring Absolute Membrane Potential Across Space and Time.

Tytuł:
Measuring Absolute Membrane Potential Across Space and Time.
Autorzy:
Lazzari-Dean JR; Department of Chemistry, University of California, Berkeley, California 94720, USA; email: , .
Gest AMM; Department of Chemistry, University of California, Berkeley, California 94720, USA; email: , .
Miller EW; Department of Chemistry, University of California, Berkeley, California 94720, USA; email: , .; Department of Molecular and Cell Biology, University of California, Berkeley, California 94720, USA.; Helen Wills Neuroscience Institute, University of California, Berkeley, California 94720, USA.
Źródło:
Annual review of biophysics [Annu Rev Biophys] 2021 May 06; Vol. 50, pp. 447-468. Date of Electronic Publication: 2021 Mar 02.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.; Review
Język:
English
Imprint Name(s):
Original Publication: Palo Alto, CA : Annual Reviews
MeSH Terms:
Membrane Potentials*
Animals ; Humans ; Intracellular Space ; Time Factors
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Grant Information:
R35 GM119855 United States GM NIGMS NIH HHS; T32 GM066698 United States GM NIGMS NIH HHS
Contributed Indexing:
Keywords: electrophysiology; fluorescence; fluorescence lifetime; membrane potential; microscopy; quantitative imaging
Entry Date(s):
Date Created: 20210302 Date Completed: 20210527 Latest Revision: 20240403
Update Code:
20240403
PubMed Central ID:
PMC8327616
DOI:
10.1146/annurev-biophys-062920-063555
PMID:
33651949
Czasopismo naukowe
Membrane potential (V mem ) is a fundamental biophysical signal present in all cells. V mem signals range in time from milliseconds to days, and they span lengths from microns to centimeters. V mem affects many cellular processes, ranging from neurotransmitter release to cell cycle control to tissue patterning. However, existing tools are not suitable for V mem quantification in many of these areas. In this review, we outline the diverse biology of V mem , drafting a wish list of features for a V mem sensing platform. We then use these guidelines to discuss electrode-based and optical platforms for interrogating V mem . On the one hand, electrode-based strategies exhibit excellent quantification but are most effective in short-term, cellular recordings. On the other hand, optical strategies provide easier access to diverse samples but generally only detect relative changes in V mem . By combining the respective strengths of these technologies, recent advances in optical quantification of absolute V mem enable new inquiries into V mem biology.

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