Optical Estimation of Membrane Potential Values Using Fluorescence Lifetime Imaging Microscopy and Hybrid Chemical-Genetic Voltage Indicators

被引:1
作者
Gest, Anneliese M. M. [1 ]
Grenier, Vincent [1 ]
Miller, Evan W. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA USA
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA USA
[3] Univ Calif Berkeley, Helen Wills Neurosci Inst, Berkeley, CA USA
[4] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
来源
BIOELECTRICITY | 2024年 / 6卷 / 01期
基金
加拿大自然科学与工程研究理事会;
关键词
fluorescence; FLIM; voltage sensitive fluorophores; CELLS; DEPOLARIZATION; PROGRESSION; GENERATION; PROTEIN;
D O I
10.1089/bioe.2023.0027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Membrane potential (Vm), the voltage across a cell membrane, is an important biophysical phenomenon, central to the physiology of cells, tissues, and organisms. Voltage-sensitive fluorescent indicators are a powerful method for interrogating membrane potential in living systems, but most indicators are best suited for detecting changes in membrane potential rather than measuring values of the membrane potential. One promising approach is to use fluorescence lifetime imaging microscopy (FLIM) in combination of chemically synthesized dyes to estimate a value of membrane potential. However, a drawback is that chemically synthesized dyes show poor specificity of staining.Objectives: To address this problem, we applied a chemical-genetic voltage imaging approach to FLIM to enable optical estimation of membrane potential values from genetically defined cells.Results: In this report, we detail the characterization and evaluation of two of these systems in mammalian cells. We further validate the use of a FLIM-based chemical genetic voltage indicator in mammalian neurons.Conclusions: Finally, we discuss opportunities for future improvements to chemical-genetic FLIM-based voltage indicators.
引用
收藏
页码:34 / 41
页数:8
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