
无数据
Smart Computational Imaging (SCI) Laboratory (https://scilaboratory.com/), Nanjing University of Science and Technology, No.200 Xiaolingwei Street, Nanjing 210094, Jiangsu, China
Smart Computational Imaging Research Institute (SCIRI) of Nanjing University of Science and Technology, Nanjing 210094, Jiangsu, China
Jiangsu Key Laboratory of Spectral Imaging & Intelligent Sense, No. 200 Xiaolingwei Street, Nanjing 210094, Jiangsu, China
*Qian Chenchenqian@njust.edu.cn
Chao Zuozuochao@njust.edu.cn
Published:2023,
Published Online:07 February 2023,
Received:23 August 2022,
Revised:27 September 2022,
Accepted:10 October 2022
Scan QR Code
Jiaming Qian, Yu Cao, Ying Bi, et al. Structured illumination microscopy based on principal component analysis. [J]. eLight, 2023,3(1).
Jiaming Qian, Yu Cao, Ying Bi, et al. Structured illumination microscopy based on principal component analysis. [J]. eLight, 2023,3(1). DOI: 10.1186/s43593-022-00035-x.
Structured illumination microscopy (SIM) is one of the powerful super-resolution modalities in bioscience with the advantages of full-field imaging and high photon efficiency. However
artifact-free super-resolution image reconstruction requires precise knowledge about the illumination parameters. The sample- and environment-dependent on-the-fly experimental parameters need to be retrieved a posteriori from the acquired data
posing a major challenge for real-time
long-term live-cell imaging
where low photobleaching
phototoxicity
and light dose are a must. In this work
we present an efficient and robust SIM algorithm based on principal component analysis (PCA-SIM). PCA-SIM is based on the observation that the ideal phasor matrix of a SIM pattern is of rank one
leading to the low complexity
precise identification of noninteger pixel wave vector and pattern phase while rejecting components that are unrelated to the parameter estimation. We demonstrate that PCA-SIM achieves non-iteratively fast
accurate (below 0.01-pixel wave vector and 0.1% of 2π relative phase under typical noise level)
and robust parameter estimation at low SNRs
which allows real-time super-resolution imaging of live cells in complicated experimental scenarios where other state-of-the-art methods inevitably fail. In particular
we provide the open-source MATLAB toolbox of our PCA-SIM algorithm and associated datasets. The combination of iteration-free reconstruction
robustness to noise
and limited computational complexity makes PCA-SIM a promising method for high-speed
long-term
artifact-free super-resolution imaging of live cells.
Structured illumination microscopy (SIM)Super-resolutionPrincipal component analysis (PCA)
J.W. Lichtman, J.-A. Conchello, Fluorescence microscopy. Nat. Methods2(12), 910-919 (2005)
M.G. Gustafsson, L. Shao, P.M. Carlton, C.R. Wang, I.N. Golubovskaya, W.Z. Cande, D.A. Agard, J.W. Sedat, Three-dimensional resolution doubling in wide-field fluorescence microscopy by structured illumination. Biophys. J.94(12), 4957-4970 (2008)
P. Kner, B.B. Chhun, E.R. Griffis, L. Winoto, M.G. Gustafsson, Superresolution video microscopy of live cells by structured illumination. Nat.Methods6(5), 339-342 (2009)
E. Abbe, Beiträge zur theorie des mikroskops und der mikroskopischen wahrnehmung. Arch. Mikrosk. Anat. 9(1), 413-468 (1873)
E. Betzig, G.H. Patterson, R. Sougrat, O.W. Lindwasser, S. Olenych, J.S. Bonifacino, M.W. Davidson, J. Lippincott-Schwartz, H.F. Hess, Imaging intracellular fluorescent proteins at nanometer resolution. Science313(5793),1642-1645 (2006)
M.J. Rust, M. Bates, X. Zhuang, Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (storm). Nat. Methods3(10), 793-796(2006)
V. Westphal, S.O. Rizzoli, M.A. Lauterbach, D. Kamin, R. Jahn, S.W. Hell,Video-rate far-field optical nanoscopy dissects synaptic vesicle movement. Science320(5873), 246-249 (2008)
M.G. Gustafsson, Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy. J Microsc198(2), 82-87 (2000)
C. Zuo, J. Sun, J. Li, J. Zhang, A. Asundi, Q. Chen, High-resolution transport-of-intensity quantitative phase microscopy with annular illumination. Sci Rep7(1), 1-22 (2017)
Y. Fan, J. Li, L. Lu, J. Sun, Y. Hu, J. Zhang, Z. Li, Q. Shen, B. Wang, R. Zhang et al., Smart computational light microscopes (sclms) of smart computational imaging laboratory (scilab). PhotoniX2(1), 1-64 (2021)
D. Li, L. Shao, B.C. Chen, X. Zhang, M. Zhang, B. Moses, D.E. Milkie, J.R. Beach, J.A. Hammer, M. Pasham et al., Extended-resolution structured illumination imaging of endocytic and cytoskeletal dynamics. Science(2015). https://doi.org/10.1126/science.aab3500https://doi.org/10.1126/science.aab3500
Y. Guo, D. Li, S. Zhang, Y. Yang, J.-J. Liu, X. Wang, C. Liu, D.E. Milkie, R.P. Moore, U.S. Tulu et al., Visualizing intracellular organelle and cytoskeletal interactions at nanoscale resolution on millisecond timescales. Cell175(5), 1430-1442 (2018)
W. Zhao, S. Zhao, L. Li, X. Huang, S. Xing, Y. Zhang, G. Qiu, Z. Han, Y. Shang, D.-E. Sun et al., Sparse deconvolution improves the resolution of livecell super-resolution fluorescence microscopy. Nat. Biotechnol. 40(4), 606-617 (2022)
A. Lal, C. Shan, P. Xi, Structured illumination microscopy image reconstruction algorithm. IEEE J. Sel. Top. Quantum. Electron. 22(4), 50-63(2016)
G. Wen, S. Li, L. Wang, X. Chen, Z. Sun, Y. Liang, X. Jin, Y. Xing, Y. Jiu, Y. Tang et al., High-fidelity structured illumination microscopy by point-spread-function engineering. Light Sci Appl10(1), 1-12 (2021)
D.P. Hoffman, E. Betzig, Tiled reconstruction improves structured illumination microscopy. BioRxiv (2020). https://doi.org/10.1101/2020.01.06.895318https://doi.org/10.1101/2020.01.06.895318
J. Demmerle, C. Innocent, A.J. North, G. Ball, M. Müller, E. Miron, A. Matsuda, I.M. Dobbie, Y. Markaki, L. Schermelleh, Strategic and practical guidelines for successful structured illumination microscopy. Nat. Protoc. 12(5), 988-1010 (2017)
X. Huang, J. Fan, L. Li, H. Liu, R. Wu, Y. Wu, L. Wei, H. Mao, A. Lal, P. Xi et al., Fast, long-term, super-resolution imaging with hessian structured illumination microscopy. Nat. Biotechnol. 36(5), 451-459 (2018)
M. Müller, V. Mönkemöller, S. Hennig, W. Hübner, T. Huser, Open-source image reconstruction of super-resolution structured illumination microscopy data in imagej. Nat. Commun. 7(1), 1-6 (2016)
S.A. Shroff, J.R. Fienup, D.R. Williams, Phase-shift estimation in sinusoidally illuminated images for lateral superresolution. J. Opt. Soc. Am. A26(2),413-424 (2009)
K. Wicker, Non-iterative determination of pattern phase in structured illumination microscopy using auto-correlations in fourier space. Opt.Express21(21), 24692-24701 (2013)
K. Wicker, O. Mandula, G. Best, R. Fiolka, R. Heintzmann, Phase optimisation for structured illumination microscopy. Opt. Express21(2),2032-2049 (2013)
X. Zhou, M. Lei, D. Dan, B. Yao, Y. Yang, J. Qian, G. Chen, P.R. Bianco, Image recombination transform algorithm for superresolution structured illumination microscopy. J. Biomed. Opt. 21(9), 096009 (2016)
A. Markwirth, M. Lachetta, V. Mönkemöller, R. Heintzmann, W. Hübner, T. Huser, M. Müller, Video-rate multi-color structured illumination microscopy with simultaneous real-time reconstruction. Nat. Commun. 10(1),1-11 (2019)
Z. Wang, T. Zhao, H. Hao, Y. Cai, K. Feng, X. Yun, Y. Liang, S. Wang, Y. Sun, P.R. Bianco et al., High-speed image reconstruction for optically sectioned,super-resolution structured illumination microscopy. Adv. Photonics4(2),026003 (2022)
C. Zuo, Q. Chen, W. Qu, A. Asundi, Phase aberration compensation in digital holographic microscopy based on principal component analysis. Opt. Lett. 38(10), 1724-1726 (2013)
K. Chu, P.J. McMillan, Z.J. Smith, J. Yin, J. Atkins, P. Goodwin, S. Wachsmann-Hogiu, S. Lane, Image reconstruction for structured-illumination microscopy with low signal level. Opt. Express22(7), 8687-8702 (2014)
C. Wang, W. Du, Q.P. Su, M. Zhu, P. Feng, Y. Li, Y. Zhou, N. Mi, Y. Zhu, D. Jiang et al., Dynamic tubulation of mitochondria drives mitochondrial network formation. Cell Res.25(10), 1108-1120 (2015)
J. Qin, Y. Guo, B. Xue, P. Shi, Y. Chen, Q.P. Su, H. Hao, S. Zhao, C. Wu, L. Yu et al., Er-mitochondria contacts promote mtdna nucleoids active transportation via mitochondrial dynamic tubulation. Nat. Commun. 11(1), 1-12 (2020)
V. Perez, B.-J. Chang, E.H.K. Stelzer, Optimal 2d-sim reconstruction by two filtering steps with richardson-lucy deconvolution. Sci. Rep. 6(1), 1-11 (2016)
D. Sage, L. Donati, F. Soulez, D. Fortun, G. Schmit, A. Seitz, R. Guiet, C. Vonesch, M. Unser, Deconvolutionlab2: an open-source software for deconvolution microscopy. Methods115, 28-41 (2017)
0
Views
0
Downloads
0
CSCD
Publicity Resources
Related Articles
Related Author
Related Institution
京公网安备11010802024621