Direct-view oblique plane microscopy

The ability to rapidly image mesoscopic samples is critically important for many areas of biological research. Owing to its high throughput and gentle, volumetric imaging nature, light-sheet fluorescence microscopy (LSFM) is an attractive modality to image such samples. However, the orthogonal dual-objective geometry of LSFM makes sample mounting challenging. Oblique plane microscopy (OPM) circumvents these issues by achieving light-sheet imaging through a single objective near the sample, with a further two objectives acting to image a tilted, oblique plane in the specimen. However, at low magnification, as required for mesoscopic imaging, conventional OPM systems suffer from a complicated and inefficient light path and/or a limited numerical aperture. Here, we present a simple method for mesoscopic OPM that enables efficient light collection at any numerical aperture. By placing the camera directly in the remote space, the oblique plane can be imaged without the need for a third microscope system. Using a commercially available camera with 1.4 µm pixels, we demonstrate imaging over a field of view with a lateral resolution of and an axial resolution of . Our technique is then used to image a 5.3×3×2.6mm 3 -expanded brain organoid.

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Publication Details

Journal
Optica
Published
2025-03-14
DOI
https://doi.org/10.1364/optica.558420
Citations
5
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
8.17
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article

Direct-view oblique plane microscopy

James D. Manton, Michael Mestre, Jacob R. Lamb, Madeline A. Lancaster
5 citations
Optica
Advanced Fluorescence Microscopy Techniques
8.17
article

Direct-view oblique plane microscopy

James D. Manton, Michael Mestre, Jacob R. Lamb, Madeline A. Lancaster
article en
5 citations

Abstract

The ability to rapidly image mesoscopic samples is critically important for many areas of biological research. Owing to its high throughput and gentle, volumetric imaging nature, light-sheet fluorescence microscopy (LSFM) is an attractive modality to image such samples. However, the orthogonal dual-objective geometry of LSFM makes sample mounting challenging. Oblique plane microscopy (OPM) circumvents these issues by achieving light-sheet imaging through a single objective near the sample, with a further two objectives acting to image a tilted, oblique plane in the specimen. However, at low magnification, as required for mesoscopic imaging, conventional OPM systems suffer from a complicated and inefficient light path and/or a limited numerical aperture. Here, we present a simple method for mesoscopic OPM that enables efficient light collection at any numerical aperture. By placing the camera directly in the remote space, the oblique plane can be imaged without the need for a third microscope system. Using a commercially available camera with 1.4 µm pixels, we demonstrate imaging over a field of view with a lateral resolution of and an axial resolution of . Our technique is then used to image a 5.3×3×2.6mm 3 -expanded brain organoid.

OpticaVol. 12(4)
Openalex Percentile: Top 3%
Advanced Fluorescence Microscopy Techniques
8.17
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Direct-view oblique plane microscopy — James D. Manton, Michael Mestre, et al. · Optica (2025) | TGRS Research Map | TGRS