Physically Constrained Signal Reconstruction for Calcium Imaging with Deep-Prior ODEs
by
OHSA/B17
Fluorescent sensors are powerful tools for studying biological signaling, designed so their brightness tracks the concentration of chemical messengers inside cells. However, the binding kinetics of these sensors are often overlooked when interpreting the resulting fluorescence data. In this talk, I’ll show how this can distort our view of cellular signals, and how accounting for it allows us to recover their true spatiotemporal dynamics. Our method fits fluorescence data under the constraints of the underlying chemical reactions, using a deep prior for temporal regularization. In calcium imaging experiments, we can reconstruct consistent calcium waveforms across different sensors and even resolve individual calcium events within a single neuron. This approach not only enhances existing sensors but also highlights how incorporating physical constraints can make computational imaging both more accurate and more insightful.
The Laboratory for Simulation and Modeling
SDSC Hub at PSI