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DOI 10.1088/1741-2552/ae4925

Медицинская библиотека · Journal of neural engineering · 2026

Computational optimization of two-photon holographic stimulation sitesin vivo.

Triplett Marcus A, Bäumler Edgar, Prodan Alex, Stonis Rokas, Peterka Darcy S, Häusser Michael, Paninski Liam

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Objective.Determining the intricate structure and function of neural circuits requires the ability to precisely manipulate circuit activity. Two-photon holographic optogenetics has emerged as a powerful tool for achieving this via flexible excitation of user-defined neural ensembles. However, the precision of two-photon optogenetics has been constrained by off-target stimulation (OTS), an effect where proximal non-target neurons can be unintentionally activated due to imperfect spatial confinement of light onto target neurons. New approaches are therefore needed to resolve the OTS problem.Approach.Here, we introduce a real-time computational method for mitigating OTS that first empirically samples each neuron's sensitivity to stimulation at proximal locations, and then optimizes stimulation sites using a fast, interpretable model based on adaptive non-negative basis function regression (NBFR).Main results.NBFR is highly scalable, completing model fitting for hundreds of neurons in just a few seconds and then optimizing stimulation sites in several hundred milliseconds per stimulus-fast enough for most closed-loop behavioral experiments. We characterize the performance of our approach in both simulations andin vivoexperiments in mouse hippocampus, showing its efficacy under realistic experimental conditions.Significance.Our results thus establish NBFR-based photostimulus optimization as an important addition to an emerging computational toolkit for precise yet scalable holographic optogenetics.

Для цитирования: Triplett Marcus A, Bäumler Edgar, Prodan Alex, Stonis Rokas, Peterka Darcy S, Häusser Michael, Paninski Liam. Computational optimization of two-photon holographic stimulation sitesin vivo.. Journal of neural engineering. 2026. DOI: 10.1088/1741-2552/ae4925.

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