Optical sectioning lattice structured illumination microscopy (OS-LSIM)

Optical sectioning structured illumination microscopy (OS-SIM) is a high-speed, minimally invasive, three-dimensional imaging microscopic technique, playing an important role in life science. However, OS-SIM is unable to achieve optical sectioning and isotropic super-resolution simultaneously. To tackle this drawback, we propose and demonstrate herein optical sectioning lattice structured illumination microscopy (OS-LSIM). This method utilizes a digital micro-mirror device to generate two-dimensional lattice patterns and a lock-in based reconstruction algorithm to realize both optical sectioning and spatial resolution enhancement. OS-LSIM features an axial resolution (optical sectioning strength) of 688 ± 16 nm and a lateral resolution improvement factor of 1.79 compared to conventional wide-field microscopy. We anticipate that OS-LSIM will open new avenues for the study of cellular dynamics in life science.

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Publication Details

Journal
Applied Physics Letters
Published
2026-04-06
DOI
https://doi.org/10.1063/5.0325196
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Optical sectioning lattice structured illumination microscopy (OS-LSIM)

Tanping Li, Kequn Zhuo, Zihan Xiong, Juanjuan Zheng et al.
Applied Physics Letters
Advanced Fluorescence Microscopy Techniques
article

Optical sectioning lattice structured illumination microscopy (OS-LSIM)

Tanping Li, Kequn Zhuo, Zihan Xiong, Juanjuan Zheng, Wenjian Wang, Kai Wen, Sha An, Peng Gao, Xiaofang Wang
article en

Abstract

Optical sectioning structured illumination microscopy (OS-SIM) is a high-speed, minimally invasive, three-dimensional imaging microscopic technique, playing an important role in life science. However, OS-SIM is unable to achieve optical sectioning and isotropic super-resolution simultaneously. To tackle this drawback, we propose and demonstrate herein optical sectioning lattice structured illumination microscopy (OS-LSIM). This method utilizes a digital micro-mirror device to generate two-dimensional lattice patterns and a lock-in based reconstruction algorithm to realize both optical sectioning and spatial resolution enhancement. OS-LSIM features an axial resolution (optical sectioning strength) of 688 ± 16 nm and a lateral resolution improvement factor of 1.79 compared to conventional wide-field microscopy. We anticipate that OS-LSIM will open new avenues for the study of cellular dynamics in life science.

Applied Physics LettersVol. 128(14)
Ministry of Education of the People's Republic of China (CN), Xidian University (CN), Nanomaterials Research (United States) (US)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Natural Science Foundation of Shaanxi Province
Responsible consumption and production
Openalex Percentile: Top 19%
Advanced Fluorescence Microscopy Techniques
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Optical sectioning lattice structured illumination microscopy (OS-LSIM) — Tanping Li, Kequn Zhuo, et al. · Applied Physics Letters (2026) | TGRS Research Map | TGRS