High-speed neural imaging with multiplexed miniaturized two-photon microscopy

Head-mounted miniaturized two-photon microscopes enable cellular-resolution recording of neural activity deep in the mouse brain during unrestrained behavior. Two-photon microscopy, however, is traditionally limited in frame rate by the necessity of scanning the excitation beam over a large field-of-view (FOV). Here, we present two types of multiplexed miniaturized two-photon microscopes (M-MINI2Ps) that preserve spatial resolution while increasing frame rate by simultaneously imaging two FOVs and demixing them temporally or computationally. We demonstrate large-scale (500 × 500 μm<sup>2</sup> FOV) multiplane calcium imaging in visual and prefrontal cortices of freely moving mice during spontaneous exploration, social behavior, and auditory stimulus. The increased speed of M-MINI2Ps also enables two-photon voltage imaging at 400 Hz over a 380 × 150 μm<sup>2</sup> FOV in freely moving mice. With compact footprints and compatibility with the open-source MINI2P, M-MINI2Ps enable high-speed recording of rapid neural dynamics and large-volume population activity in freely moving mice, providing a powerful tool for systems neuroscience.

Authors

Institutions

Publication Details

Journal
Cell Reports Methods
Published
2025-11-11
DOI
https://doi.org/10.1016/j.crmeth.2025.101221
Citations
3
Primary Topic
Neural dynamics and brain function
Type
article
Field-Weighted Citation Impact
4.29
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

High-speed neural imaging with multiplexed miniaturized two-photon microscopy

J. Muir, Zixiao Zhang, Shing-Jiuan Liu, Christina K. Kim et al.
3 citations
Cell Reports Methods
Neural dynamics and brain function
4.29
article

High-speed neural imaging with multiplexed miniaturized two-photon microscopy

J. Muir, Zixiao Zhang, Shing-Jiuan Liu, Christina K. Kim, Ben Mattison, Weijian Yang, Noah Spurr
article en
3 citations

Abstract

Head-mounted miniaturized two-photon microscopes enable cellular-resolution recording of neural activity deep in the mouse brain during unrestrained behavior. Two-photon microscopy, however, is traditionally limited in frame rate by the necessity of scanning the excitation beam over a large field-of-view (FOV). Here, we present two types of multiplexed miniaturized two-photon microscopes (M-MINI2Ps) that preserve spatial resolution while increasing frame rate by simultaneously imaging two FOVs and demixing them temporally or computationally. We demonstrate large-scale (500 × 500 μm<sup>2</sup> FOV) multiplane calcium imaging in visual and prefrontal cortices of freely moving mice during spontaneous exploration, social behavior, and auditory stimulus. The increased speed of M-MINI2Ps also enables two-photon voltage imaging at 400 Hz over a 380 × 150 μm<sup>2</sup> FOV in freely moving mice. With compact footprints and compatibility with the open-source MINI2P, M-MINI2Ps enable high-speed recording of rapid neural dynamics and large-volume population activity in freely moving mice, providing a powerful tool for systems neuroscience.

Cell Reports MethodsVol. 5(12)
University of California, Davis (US)
Openalex Percentile: Top 5%
Neural dynamics and brain function
4.29
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

High-speed neural imaging with multiplexed miniaturized two-photon microscopy — J. Muir, Zixiao Zhang, et al. · Cell Reports Methods (2025) | TGRS Research Map | TGRS