Linearly polarized excitation enhances signals from fluorescent voltage indicators

Journal Article (2021)
Author(s)

William Bloxham (Harvard University, Massachusetts Institute of Technology)

Daan Brinks (TU Delft - ImPhys/Microscopy Instrumentation & Techniques, Harvard University)

Simon Kheifets (Harvard University)

Adam E. Cohen (Harvard University)

Research Group
ImPhys/Microscopy Instrumentation & Techniques
DOI related publication
https://doi.org/10.1016/j.bpj.2021.10.028 Final published version
More Info
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Publication Year
2021
Language
English
Research Group
ImPhys/Microscopy Instrumentation & Techniques
Issue number
23
Volume number
120
Pages (from-to)
5333-5342
Downloads counter
176

Abstract

Voltage imaging in cells requires high-speed recording of small fluorescent signals, often leading to low signal/noise ratios. Because voltage indicators are membrane bound, their orientations are partially constrained by the plane of the membrane. We explored whether tuning the linear polarization of excitation light could enhance voltage indicator fluorescence. We tested a panel of dye- and protein-based voltage indicators in mammalian cells. The dye BeRST1 showed a 73% increase in brightness between the least and most favorable polarizations. The protein-based reporter ASAP1 showed a 22% increase in brightness, and QuasAr3 showed a 14% increase in brightness. In very thin neurites expressing QuasAr3, improvements were anomalously large, with a 170% increase in brightness between polarization parallel versus perpendicular to the dendrite. Signal/noise ratios of optically recorded action potentials were increased by up to 50% in neurites expressing QuasAr3. These results demonstrate that polarization control can be a facile means to enhance signals from fluorescent voltage indicators, particularly in thin neurites or in high-background environments.