1.Smart Computational Imaging (SCI) Laboratory, Nanjing University of Science and Technology, Nanjing, Jiangsu Province 210094, China
2.Smart Computational Imaging Research Institute (SCIRI) of Nanjing University of Science and Technology, Nanjing, Jiangsu Province 210094, China
3.Jiangsu Key Laboratory of Spectral Imaging & Intelligent Sense, Nanjing University of Science and Technology, Nanjing, Jiangsu Province 210094, China
Qian Chen (chenqian@njust.edu.cn)
Chao Zuo (zuochao@njust.edu.cn)
收稿:2024-12-31,
修回:2025-06-07,
录用:2025-07-22,
网络出版:2025-09-01,
纸质出版:2025-10-31
Scan QR Code
Jiaming Qian, Weiyi Xia, Yuxia Huang, 等. Principal component analysis for three-dimensional structured illumination microscopy (PCA-3DSIM)[J]. Light: Science & Applications, 2025,14(10):3170-3181.
Qian, J. M. et al. Principal component analysis for three-dimensional structured illumination microscopy (PCA-3DSIM). Light: Science & Applications, 14, 3170-3181 (2025).
Jiaming Qian, Weiyi Xia, Yuxia Huang, 等. Principal component analysis for three-dimensional structured illumination microscopy (PCA-3DSIM)[J]. Light: Science & Applications, 2025,14(10):3170-3181. DOI: 10.1038/s41377-025-01979-8.
Qian, J. M. et al. Principal component analysis for three-dimensional structured illumination microscopy (PCA-3DSIM). Light: Science & Applications, 14, 3170-3181 (2025). DOI: 10.1038/s41377-025-01979-8.
Three-dimensional structured illumination microscopy (3DSIM) is an essential super-resolution imaging technique for visualizing volumetric subcellular structures at the nanoscale
capable of doubling both lateral and axial resolution beyond the diffraction limit. However
high-quality 3DSIM reconstruction is often hindered by uncertainties in experimental parameters
such as optical aberrations and fluorescence density heterogeneity. Here
we present PCA-3DSIM
a novel 3DSIM reconstruction framework that extends principal component analysis (PCA) from two-dimensional (2D) to three-dimensional (3D) super-resolution microscopy. To further compensate spatial nonuniformities of illumination parameters
PCA-3DSIM can be implemented in an adaptive tiled-block manner. By segmenting raw volumetric data into localized subsets
PCA-3DSIM enables accurate parameter estimation and effective interference rejection for high-fidelity
artifact-free 3D super-resolution reconstruction
with the inherent efficiency of PCA supporting the tiled reconstruction with limited computational burden. Experimental results demonstrate that PCA-3DSIM provides reliable reconstruction performance and improved robustness across diverse imaging scenarios
from custom-built platforms to commercial systems. These results establish PCA-3DSIM as a flexible and practical tool for super-resolved volumetric imaging of subcellular structures
with broad potential applications in biomedical research.
Abbe, E. Beiträge zur Theorie des Mikroskops und der mikroskopischen Wahrnehmung. Arch. Mikroskopische Anat . 9 , 413–468 (1873)..
Sun, Y. L. et al. Fluorescence interference structured illumination microscopy for 3D morphology imaging with high axial resolution. Adv. Photonics 5 , 056007 (2023)..
Liu, W. J. et al. Three-dimensional super-resolution imaging of live whole cells using galvanometer-based structured illumination microscopy. Opt. Express 27 , 7237–7248 (2019)..
Zhang, Y. W. et al. Super-resolution algorithm based on Richardson-Lucy deconvolution for three-dimensional structured illumination microscopy. J. Optical Soc. Am. A 36 , 173–178 (2019)..
Gustafsson, M. G. L. Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy. J. Microsc . 198 , 82–87 (2000)..
Gustafsson, M. G. L. et al. Three-dimensional resolution doubling in wide-field fluorescence microscopy by structured illumination. Biophys. J . 94 , 4957–4970 (2008)..
Shao, L. et al. I 5 S: wide-field light microscopy with 100-nm-scale resolution in three dimensions. Biophys. J . 94 , 4971–4983 (2008)..
Shao, L. et al. Super-resoluti on 3D microscopy of live whole cells using structured illumination. Nat. Methods 8 , 1044–1046 (2011)..
Fiolka, R. et al. Time-lapse two-color 3D imaging of live cells with doubled resolution using structured illumination. Proc. Natl Acad. Sci. USA 109 , 5311–5315 (2012)..
Lin, R. Z. et al. Subcellular three-dimensional imaging deep through multicellular thick samples by structured illumination microscopy and adaptive optics. Nat. Commun . 12 , 3148 (2021)..
Carlton, P. M. Three-dimensional structured illumination microscopy and its application to chromosome structure. Chromosome Res . 16 , 351–365 (2008)..
Shu, Y. F. et al. Adaptive optical quantitative phase imaging based on annular illumination Fourier ptychographic microscopy. PhotoniX 3 , 24 (2022)..
Chen, X. et al. Superresolution structured illumination microscopy reconstruction algorithms: a review. Light Sci. Appl . 12 , 172 (2023)..
Zhao, T. Y. et al. Fast single-layer reconstruction for three-dimensional structured illumination microscopy. Opt. Lasers Eng . 167 , 107606 (2023)..
Müller, M. et al. Open-source image reconstruction of super-resolution structured illumination microscopy data in ImageJ. Nat. Commun . 7 , 10980 (2016)..
Wang, Z. J. et al. High-speed image reconstruction for optically sectioned, super-resolution structured illumination microscopy. Adv. Photonics 4 , 026003 (2022)..
O'Connell, C. B. Live cell super-resolution imaging with N-SIM. Microsc. Today 20 , 18–21 (2012)..
Li, X. S. et al. Three-dimensional structured illumination microscopy with enhanced axial resolution. Nat. Biotechnol . 41 , 1307–1319 (2023)..
Cao, R. J. et al. Open-3DSIM: an open-source three-dimensional structured illumination microscopy reconstruction platform. Nat. Methods 20 , 1183–1186 (2023)..
Demmerle, J. et al. Strategic and practical guidelines for successful structured illumination microscopy. Nat. Protoc . 12 , 988–1010 (2017)..
Wen, G. et al. High-fidelity structured illumination microscopy by point-spread-function engineering. Light Sci. Appl . 10 , 70 (2021)..
Huang, X. S. et al. Fast, long-term, super-resolution imaging with Hessian structured illumination microscopy. Nat. Biotechnol . 36 , 451–459 (2018)..
Zhao, W. S. et al. Sparse deconvolution improves the resolution of live-cell super-resolution fluorescence microscopy. Nat. Biotechnol . 40 , 606–617 (2022)..
Chu, K. Q. et al. Image reconstruction for structured-illumination microscopy with low signal level. Opt. Express 22 , 8687–8702 (2014)..
Hou, Y. W. et al. Multi-resolution analysis enables fidelity-ensured deconvolution for fluorescence microscopy. eLight 4 , 14 (2024)..
Hoffman, D. P. & Betzig, E. Tiled reconstruction improves structured illumination microscopy. Print at https://doi.org/10.1101/2020.01.06.895318 https://doi.org/10.1101/2020.01.06.895318 (2020).
Gibson, S. F. & Lanni, F. Experimental test of an analytical model of aberration in an oil-immersion objective lens used in three-dimensional light microscopy. J. Optical Soc. Am. A 9 , 154–166 (1992)..
Diaspro, A., Federici, F. & Robello, M. Influence of refractive-index mismatch in high-resolution three-dimensional confocal microscopy. Appl. Opt . 41 , 685–690 (2002)..
Débarre, D. et al. Image-based adaptive optics for two-photon microscopy. Opt. Lett . 34 , 2495–2497 (2009)..
Simmonds, R. Adaptive Optics for Microscopy and Photonic Engineering . Ph. D. thesis (University of Oxford, 2012).
Preibisch, S., Saalfeld, S. & Tomancak, P. Globally optimal stitching of tiled 3D microscopic image acquisitions. Bioinformatics 25 , 1463–1465 (2009)..
Johnson, K. A. & Hagen, G. M. Artifact-free whole-slide imaging with structured illumination microscopy and Bayesian image reconstruction. Gigascience 9 , giaa035 (2020)..
Qian, J. M. et al. Structured illumination microscopy based on principal componentanalysis. eLight 3 , 4 (2023)..
Shi, Q. Q., Lu, H. P. & Cheung, Y. M. Tensor rank estimation and completion via CP-based nuclear norm. In: Proc. ACM on Conference on Information and Knowledge Management . Singapore, Singapore: Association for Computing Machinery, 2017, 949–958.
Hoge, W. S. & Westin, C. F. Identification of translational displacements between N-dimensional data sets using the high-order SVD and phase correlation. IEEE Trans. Image Process . 14 , 884–889 (2005)..
De Lathauwer, L., De Moor, B. & Vandewalle, J. A multilinear singular value decomposition. SIAM J. Matrix Anal. Appl . 21 , 1253–1278 (2000)..
Lyu, J. M. et al. Motion-resistant structured illumination microscopy based on principal component analysis. Opt. Lett . 48 , 175–178 (2023)..
Liu, Y., Lauderdale, J. D. & Kner, P. Stripe artifact reduction for digital scanned structured illumination light sheet microscopy. Opt. Lett . 44 , 2510–2513 (2019)..
Ball, G. et al. SIMcheck: a toolbox for successful super-resolution structured illumination microscopy. Sci. Rep . 5 , 15915 (2015)..
Smith, C. S. et al. Structured illumination microscopy with noise-controlled image reconstructions. Nat. Methods 18 , 821–828 (2021)..
Hoge, W. S. A subspace identification extension to the phase correlation method [MRI application ] . IEEE Trans. Med. Imaging 22 , 277–280 (2003)..
Porter, T. & Duff, T. Compositing digital images. ACM SIGGRAPH Comput. Graph . 18 , 253–259 (1984)..
Christensen, C. M. Exploring the limits of the technology S-curve. Part Ⅰ: component technologies. Prod. Oper. Manag . 1 , 334–357 (1992)..
Zhao, W. S. et al. Quantitatively mapping local quality of super-resolution microscopy by rolling Fourier ring correlation. Light Sci. Appl . 12 , 298 (2023)..
Culley, S. et al. Quantitative mapping and minimization of super-resolution optical imaging artifacts. Nat. Methods 15 , 263–266 (2018)..
0
浏览量
0
Downloads
0
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010802024621