Self-supervised denoising for multimodal structured illumination microscopy enables long-term super-resolution live-cell imaging

被引:0
|
作者
Xingye Chen
Chang Qiao
Tao Jiang
Jiahao Liu
Quan Meng
Yunmin Zeng
Haoyu Chen
Hui Qiao
Dong Li
Jiamin Wu
机构
[1] Tsinghua University,Department of Automation
[2] Beihang University,Research Institute for Frontier Science
[3] Tsinghua University,Institute for Brain and Cognitive Sciences
[4] Chinese Academy of Sciences,National Laboratory of Biomacromolecules, New Cornerstone Science Laboratory, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics
[5] University of Chinese Academy of Sciences,College of Life Sciences
[6] Huazhong University of Science and Technology,Laboratory of Image Processing and Intelligent Control of Ministry of Education of China, School of Artificial Intelligence and Automation
来源
PhotoniX | / 5卷
关键词
Super-resolution microscopy; Structured illumination microscopy; Deep learning; Self-supervised learning; Live-cell imaging;
D O I
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中图分类号
学科分类号
摘要
Detection noise significantly degrades the quality of structured illumination microscopy (SIM) images, especially under low-light conditions. Although supervised learning based denoising methods have shown prominent advances in eliminating the noise-induced artifacts, the requirement of a large amount of high-quality training data severely limits their applications. Here we developed a pixel-realignment-based self-supervised denoising framework for SIM (PRS-SIM) that trains an SIM image denoiser with only noisy data and substantially removes the reconstruction artifacts. We demonstrated that PRS-SIM generates artifact-free images with 20-fold less fluorescence than ordinary imaging conditions while achieving comparable super-resolution capability to the ground truth (GT). Moreover, we developed an easy-to-use plugin that enables both training and implementation of PRS-SIM for multimodal SIM platforms including 2D/3D and linear/nonlinear SIM. With PRS-SIM, we achieved long-term super-resolution live-cell imaging of various vulnerable bioprocesses, revealing the clustered distribution of Clathrin-coated pits and detailed interaction dynamics of multiple organelles and the cytoskeleton.
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