A new single-objective light-sheet microscope has been developed that uses novel optics and imaging protocols to increase resolution without compromising imaging speed and volume.
This is a preview of subscription content, access via your institution
Access options
Access Nature and 54 other Nature Portfolio journals
Get Nature+, our best-value online-access subscription
$29.99 / 30 days
cancel any time
Subscribe to this journal
Receive 12 print issues and online access
$259.00 per year
only $21.58 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
Dunsby, C. Optically sectioned imaging by oblique plane microscopy. Optics Express 16, 20306–20316 (2008). Seminal paper that presents oblique plane microscopy (OPM), the first demonstration of single-objective light-sheet microscopy with no additional reflecting elements.
Bouchard, M. B. et al. Swept confocally-aligned planar excitation (SCAPE) microscopy for high-speed volumetric imaging of behaving organisms. Nat. Photonics 9, 113–119 (2015). This paper reports SCAPE, a single-objective light-sheet microscope that allows volumetric imaging of living samples at ultrafast speeds.
Yang, B. et al. Epi-illumination SPIM for volumetric imaging with high spatial-temporal resolution. Nat. Methods 16, 501–504 (2019). This work solved the long-standing resolution-loss problem in OPM and demonstrated uncompromised spatial resolution for subcellular imaging.
Millett-Sikking, A. et al. High NA single-objective light-sheet. https://andrewgyork.github.io/high_na_single_objective_lightsheet/ (accessed 28 Jan 2022). An ongoing project that reports the use of a custom glass-tipped objective lens for high-resolution, single-objective light-sheet microscopy — a critical step towards widespread adoption.
Sapoznik, E. et al. A versatile oblique plane microscope for large-scale and high-resolution imaging of subcellular dynamics. Elife 9, e57681 (2020). Demonstrates high-resolution, subcellular single-objective light-sheet imaging of living specimens mounted in a variety of imaging chambers, including microfluidic devices.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
This is a summary of: Yang, B. et al. DaXi—high-resolution, large imaging volume and multi-view single-objective light-sheet microscopy. Nat. Methods https://doi.org/10.1038/s41592-022-01417-2 (2022)
Rights and permissions
About this article
Cite this article
DaXi: pushing the limits of single-objective light-sheet microscopy. Nat Methods 19, 414–415 (2022). https://doi.org/10.1038/s41592-022-01420-7
Published:
Issue Date:
DOI: https://doi.org/10.1038/s41592-022-01420-7