Voltage Imaging with a NIR-Absorbing Phosphine Oxide Rhodamine Voltage Reporter

The development of fluorescent dyes that emit and absorb light at wavelengths greater than 700 nm and that respond to biochemical and biophysical events in living systems remains an outstanding challenge for noninvasive optical imaging. Here, we report the design, synthesis, and application of near-...

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Veröffentlicht in:Journal of the American Chemical Society 2021-02, Vol.143 (5), p.2304-2314
Hauptverfasser: Gonzalez, Monica A, Walker, Alison S, Cao, Kevin J, Lazzari-Dean, Julia R, Settineri, Nicholas S, Kong, Eui Ju, Kramer, Richard H, Miller, Evan W
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container_end_page 2314
container_issue 5
container_start_page 2304
container_title Journal of the American Chemical Society
container_volume 143
creator Gonzalez, Monica A
Walker, Alison S
Cao, Kevin J
Lazzari-Dean, Julia R
Settineri, Nicholas S
Kong, Eui Ju
Kramer, Richard H
Miller, Evan W
description The development of fluorescent dyes that emit and absorb light at wavelengths greater than 700 nm and that respond to biochemical and biophysical events in living systems remains an outstanding challenge for noninvasive optical imaging. Here, we report the design, synthesis, and application of near-infrared (NIR)-absorbing and -emitting optical voltmeter based on a sulfonated, phosphine-oxide (po) rhodamine for voltage imaging in intact retinas. We find that po-rhodamine based voltage reporters, or poRhoVRs, display NIR excitation and emission profiles at greater than 700 nm, show a range of voltage sensitivities (13 to 43% ΔF/F per 100 mV in HEK cells), and can be combined with existing optical sensors, like Ca2+-sensitive fluorescent proteins (GCaMP), and actuators, like light-activated opsins ChannelRhodopsin-2 (ChR2). Simultaneous voltage and Ca2+ imaging reveals differences in activity dynamics in rat hippocampal neurons, and pairing poRhoVR with blue-light based ChR2 affords all-optical electrophysiology. In ex vivo retinas isolated from a mouse model of retinal degeneration, poRhoVR, together with GCaMP-based Ca2+ imaging and traditional multielectrode array (MEA) recording, can provide a comprehensive physiological activity profile of neuronal activity, revealing differences in voltage and Ca2+ dynamics within hyperactive networks of the mouse retina. Taken together, these experiments establish that poRhoVR will open new horizons in optical interrogation of cellular and neuronal physiology in intact systems.
doi_str_mv 10.1021/jacs.0c11382
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subjects Animals
Calcium - metabolism
Fluorescent Dyes - chemistry
Fluorescent Dyes - metabolism
Infrared Rays
Mice
Neurons - cytology
Neurons - metabolism
Optical Imaging
Oxides - chemistry
Phosphines - chemistry
Retina - cytology
Retina - diagnostic imaging
Retina - metabolism
Rhodamines - chemistry
title Voltage Imaging with a NIR-Absorbing Phosphine Oxide Rhodamine Voltage Reporter
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