High-spatiotemporal-throughput video microscopy of freely moving organisms with diffractive multiplexing across a sensor array
Conventional microscopes exhibit a tradeoff among spatial resolution, field of view (FOV), and frame rate. To overcome this tradeoff, we designed a highly parallelized and multiplexed computational microscope that increases the spatiotemporal throughput by two orders of magnitude, achieving tens of gigapixels per second. Specifically, our microscope features a non-contiguous array of 48 camera sensors, with the information in the gaps multiplexed across the sensor array via an optimized diffractive pupil in a single synchronized snapshot. We applied our computational microscope to image dozens of freely-moving C. elegans in parallel at few-micron resolution over a multi-cm2 FOV at up to 40 fps.
Authors
- Kevin C. Zhou (ORCID: https://orcid.org/0000-0002-0351-8812)
- Laura Waller (ORCID: https://orcid.org/0000-0003-1243-2356)
- Saul Kato (ORCID: https://orcid.org/0000-0003-2990-8306)
- Rajesh Menon (ORCID: https://orcid.org/0000-0002-4777-376X)
- Muneki Ikeda (ORCID: https://orcid.org/0000-0003-3063-5683)
- Tina Hayward
- Nicholas Antipa
- Roarke Horstmeyer (ORCID: https://orcid.org/0000-0002-2480-9141)
- Chaoying Gu (ORCID: https://orcid.org/0009-0009-9266-6785)
Institutions
- Duke University (US)
- University of California, San Francisco (US)
- University of Utah (US)
- University of California San Diego (US)
- University of California, Berkeley (US)
Publication Details
- Published
- 2025-03-19
- DOI
- https://doi.org/10.1117/12.3042628
- Citations
- 1
- Primary Topic
- Advanced Fluorescence Microscopy Techniques
- Type
- article
- Field-Weighted Citation Impact
- 1.63