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.
Authors
- Tanping Li (ORCID: https://orcid.org/0000-0002-2164-2673)
- Kequn Zhuo
- Zihan Xiong
- Juanjuan Zheng
- Wenjian Wang
- Kai Wen
- Sha An
- Peng Gao
- Xiaofang Wang
Institutions
- Ministry of Education of the People's Republic of China (CN)
- Xidian University (CN)
- Nanomaterials Research (United States) (US)
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
Funders
- National Natural Science Foundation of China
- China Postdoctoral Science Foundation
- Natural Science Foundation of Shaanxi Province