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New Molecular Scaffolds for Fluorescent Voltage Indicators.


ABSTRACT: The ability to non-invasively monitor membrane potential dynamics in excitable cells like neurons and cardiomyocytes promises to revolutionize our understanding of the physiology and pathology of the brain and heart. Here, we report the design, synthesis, and application of a new class of fluorescent voltage indicators that make use of a fluorene-based molecular wire as a voltage-sensing domain to provide fast and sensitive measurements of membrane potential in both mammalian neurons and human-derived cardiomyocytes. We show that the best of the new probes, fluorene VoltageFluor 2 (fVF 2), readily reports on action potentials in mammalian neurons, detects perturbations to the cardiac action potential waveform in human induced pluripotent stem cell-derived cardiomyocytes, shows a substantial decrease in phototoxicity compared to existing molecular wire-based indicators, and can monitor cardiac action potentials for extended periods of time. Together, our results demonstrate the generalizability of a molecular wire approach to voltage sensing and highlight the utility of fVF 2 for interrogating membrane potential dynamics.

SUBMITTER: Boggess SC 

PROVIDER: S-EPMC6499379 | biostudies-literature | 2019 Mar

REPOSITORIES: biostudies-literature

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New Molecular Scaffolds for Fluorescent Voltage Indicators.

Boggess Steven C SC   Gandhi Shivaani S SS   Siemons Brian A BA   Huebsch Nathaniel N   Healy Kevin E KE   Miller Evan W EW  

ACS chemical biology 20190208 3


The ability to non-invasively monitor membrane potential dynamics in excitable cells like neurons and cardiomyocytes promises to revolutionize our understanding of the physiology and pathology of the brain and heart. Here, we report the design, synthesis, and application of a new class of fluorescent voltage indicators that make use of a fluorene-based molecular wire as a voltage-sensing domain to provide fast and sensitive measurements of membrane potential in both mammalian neurons and human-d  ...[more]

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