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Bayless-Edwards, L.

Publications and source records attributed to Bayless-Edwards, L..

3 recordsLinked to original sources

iFLiP: accessible and low-cost lifetime fiber photometry for robust longitudinal and quantitative measurements of neural dynamics

Fluorescence lifetime measurements overcome the limitation of widely used intensity-based measurements in quantifying tonic activities and longitudinal changes in neural dynamics. However, while lifetime sensors are rapidly emerging, their applications have been limited by the complexity and expense of required hardware and software. Here, we report a simple, low-cost lifetime fiber photometry system, named iFLiP, that uses entirely off-the-shelf products and can be assembled without specialized expertise. We also develop software that enables turn-key operation. The integrated system can accurately monitor lifetime changes at up to 5000 Hz for days. We demonstrate the utility of iFLiP in monitoring the activity of protein kinase A (PKA) in vitro and in vivo, and uncover striatal subregion- and cell-type-specific PKA dynamics elicited by locomotion in mice. Additionally, multi-day continuous measurements in the basal forebrain reveal previously unappreciated PKA activity associated with sleep/wakefulness. Overall, iFLiP may make lifetime measurements broadly accessible in neuroscience research.

neuroscience↗

A high-performance genetically encoded sensor for cellular imaging of PKC activity in vivo

We report a genetically encoded fluorescence lifetime sensor for protein kinase C (PKC) activity, named CKAR3, based on Forster resonance energy transfer. CKAR3 exhibits a 10-fold increased dynamic range compared to its parental sensors and enables in vivo imaging of PKC activity during animal behavior. Our results reveal robust PKC activity in a sparse neuronal subset in the motor cortex during locomotion, in part mediated by muscarinic acetylcholine receptors.

neuroscience↗

Highly sensitive genetically-encoded sensors for population and subcellular imaging of cAMP in vivo

Cyclic adenosine monophosphate (cAMP) integrates information from diverse G protein-coupled receptors, such as neuromodulator receptors, to regulate pivotal biological processes in a cellular- and subcellular-specific manner. However, in vivo cellular-resolution imaging of cAMP dynamics in neurons has not been demonstrated. Here, we screen existing genetically-encoded cAMP sensors, and further develop the best performer to derive three improved variants, called cAMPFIREs. These sensors exhibit up to ten-fold increased sensitivity to cAMP and a corrected, cytosolic distribution. cAMPFIREs are compatible with both ratiometric and fluorescence lifetime imaging, and can detect cAMP dynamics elicited by norepinephrine at physiologically-relevant, nanomolar concentrations. Imaging of cAMPFIREs in awake mice reveals tonic levels of cAMP in cortical neurons that are associated with wakefulness, and are differentially regulated in different subcellular compartments. Furthermore, enforced locomotion elicits neuron-specific, bidirectional cAMP dynamics, in part, mediated by norepinephrine. Finally, cAMPFIREs also function in Drosophila, suggesting that they have broad applicability for studying intracellular signaling in vivo.

neuroscience↗