Circularly permuted green fluorescent protein (cpGFP)-based high-performance cAMP sensors have enabled real-time monitoring of cAMP dynamics with high spatiotemporal resolution in living animals. However, their utility is hampered by significant spectral overlap with other green/yellow fluorescent indicators and blue/cyan light-activated optogenetic actuators, limiting their compatibility in multiplexed imaging applications. While existing red cAMP sensors offer great spectral separation, they often suffer from a limited dynamic range ( 10-fold in HEK293T cells), enhanced cellular brightness, appropriate cAMP affinity (Kd ~1.9 μM), subsecond response kinetics, and minimal photoactivation under blue or cyan light exposure. Using R-Flamp1, we visualized region-specific cAMP dynamics, and when paired with green indicators, revealed differential activation patterns between cAMP and neuromodulators or calcium using two-photon imaging and fiber photometry during various behaviors. These findings provide valuable insights into the role of cAMP signaling in complex behaviors. R-Flamp1 is a high-performance red fluorescent cAMP sensor and the authors monitor region-specific cAMP dynamics in vivo and reveal distinct activation patterns between cAMP, calcium, and neuromodulators via two-photon imaging and fiber photometry in animals.
Wang et al. (Mon,) studied this question.