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Increasing the Field-of-View in Oblique Plane Microscopy via optical tiling

Bingying Chen, Bo-Jui Chang, Felix Zhou, View ORCID ProfileStephan Daetwyler, Etai Sapoznik, Gabriel M. Gihana, Lizbeth Perez Castro, View ORCID ProfileMaralice Conacci Sorrell, Kevin M. Dean, Alfred Millett-Sikking, Andrew G. York, Reto Fiolka
doi: https://doi.org/10.1101/2022.06.12.495844
Bingying Chen
1Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, Texas, USA
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Bo-Jui Chang
1Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, Texas, USA
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Felix Zhou
1Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, Texas, USA
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Stephan Daetwyler
1Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, Texas, USA
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  • ORCID record for Stephan Daetwyler
Etai Sapoznik
1Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, Texas, USA
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Gabriel M. Gihana
1Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, Texas, USA
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Lizbeth Perez Castro
2Department of Cell Biology, UT Southwestern Medical Center, Dallas, Texas, USA
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Maralice Conacci Sorrell
2Department of Cell Biology, UT Southwestern Medical Center, Dallas, Texas, USA
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  • ORCID record for Maralice Conacci Sorrell
Kevin M. Dean
1Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, Texas, USA
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Alfred Millett-Sikking
3Calico Life Sciences LLC, South San Francisco, CA, USA
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Andrew G. York
3Calico Life Sciences LLC, South San Francisco, CA, USA
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Reto Fiolka
1Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, Texas, USA
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  • For correspondence: Reto.Fiolka@UTSouthwestern.edu
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Abstract

Fast volumetric imaging of large fluorescent samples with high-resolution is required for many biological applications. Oblique plane microscopy (OPM) provides high spatiotemporal resolution, but the field of view is typically limited by its optical train and the pixel number of the camera. Mechanically scanning the sample or decreasing the overall magnification of the imaging system can partially address this challenge, albeit by reducing the volumetric imaging speed or spatial sampling, respectively. In this Letter, we introduce a novel dual-axis scan unit for OPM that enables rapid and high-resolution volumetric imaging throughout a volume of 800 × 500 × 200 microns. This enables imaging of model organisms, such as zebrafish embryos, with subcellular resolution. Furthermore, we combined this microscope with a real-time and multi-perspective projection imaging technique to increase the volumetric interrogation rate to more than 10 Hz.

Competing Interest Statement

The authors have declared no competing interest.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted June 13, 2022.
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Increasing the Field-of-View in Oblique Plane Microscopy via optical tiling
Bingying Chen, Bo-Jui Chang, Felix Zhou, Stephan Daetwyler, Etai Sapoznik, Gabriel M. Gihana, Lizbeth Perez Castro, Maralice Conacci Sorrell, Kevin M. Dean, Alfred Millett-Sikking, Andrew G. York, Reto Fiolka
bioRxiv 2022.06.12.495844; doi: https://doi.org/10.1101/2022.06.12.495844
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Increasing the Field-of-View in Oblique Plane Microscopy via optical tiling
Bingying Chen, Bo-Jui Chang, Felix Zhou, Stephan Daetwyler, Etai Sapoznik, Gabriel M. Gihana, Lizbeth Perez Castro, Maralice Conacci Sorrell, Kevin M. Dean, Alfred Millett-Sikking, Andrew G. York, Reto Fiolka
bioRxiv 2022.06.12.495844; doi: https://doi.org/10.1101/2022.06.12.495844

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