TY - JOUR
T1 - All-optical closed-loop voltage clamp for precise control of muscles and neurons in live animals
AU - Bergs, Amelie C. F.
AU - Liewald, Jana F.
AU - Rodriguez-Rozada, Silvia
AU - Liu, Qiang
AU - Wirt, Christin
AU - Bessel, Artur
AU - Zeitzschel, Nadja
AU - Durmaz, Hilal
AU - Nozownik, Adrianna
AU - Dill, Holger
AU - Jospin, Maëlle
AU - Vierock, Johannes
AU - Bargmann, Cornelia I.
AU - Hegemann, Peter
AU - Wiegert, J. Simon
AU - Gottschalk, Alexander
PY - 2023
Y1 - 2023
N2 - Excitable cells can be stimulated or inhibited by optogenetics. Since optogenetic actuation regimes are often static, neurons and circuits can quickly adapt, allowing perturbation, but not true control. Hence, we established an optogenetic voltage-clamp (OVC). The voltage-indicator QuasAr2 provides information for fast, closed-loop optical feedback to the bidirectional optogenetic actuator BiPOLES. Voltage-dependent fluorescence is held within tight margins, thus clamping the cell to distinct potentials. We established the OVC in muscles and neurons of Caenorhabditis elegans, and transferred it to rat hippocampal neurons in slice culture. Fluorescence signals were calibrated to electrically measured potentials, and wavelengths to currents, enabling to determine optical I/V-relationships. The OVC reports on homeostatically altered cellular physiology in mutants and on Ca2+-channel properties, and can dynamically clamp spiking in C. elegans. Combining non-invasive imaging with control capabilities of electrophysiology, the OVC facilitates high-throughput, contact-less electrophysiology in individual cells and paves the way for true optogenetic control in behaving animals. © The Author(s) 2023.
AB - Excitable cells can be stimulated or inhibited by optogenetics. Since optogenetic actuation regimes are often static, neurons and circuits can quickly adapt, allowing perturbation, but not true control. Hence, we established an optogenetic voltage-clamp (OVC). The voltage-indicator QuasAr2 provides information for fast, closed-loop optical feedback to the bidirectional optogenetic actuator BiPOLES. Voltage-dependent fluorescence is held within tight margins, thus clamping the cell to distinct potentials. We established the OVC in muscles and neurons of Caenorhabditis elegans, and transferred it to rat hippocampal neurons in slice culture. Fluorescence signals were calibrated to electrically measured potentials, and wavelengths to currents, enabling to determine optical I/V-relationships. The OVC reports on homeostatically altered cellular physiology in mutants and on Ca2+-channel properties, and can dynamically clamp spiking in C. elegans. Combining non-invasive imaging with control capabilities of electrophysiology, the OVC facilitates high-throughput, contact-less electrophysiology in individual cells and paves the way for true optogenetic control in behaving animals. © The Author(s) 2023.
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U2 - 10.1038/s41467-023-37622-6
DO - 10.1038/s41467-023-37622-6
M3 - RGC 21 - Publication in refereed journal
C2 - 37024493
SN - 2041-1723
VL - 14
JO - Nature Communications
JF - Nature Communications
M1 - 1939
ER -