Deep learning massively accelerates super-resolution localization microscopy

被引:446
作者
Ouyang, Wei [1 ,2 ,3 ]
Aristov, Andrey [1 ,2 ,3 ]
Lelek, Mickael [1 ,2 ,3 ]
Hao, Xian [1 ,2 ,3 ]
Zimmer, Christophe [1 ,2 ,3 ]
机构
[1] Inst Pasteur, Unite Imagerie & Modelisat, Paris, France
[2] CNRS, UMR 3691, Paris, France
[3] CNRS, USR 3756, IP, C3BI, Paris, France
关键词
OPTICAL RECONSTRUCTION MICROSCOPY; NEURAL-NETWORKS; PORE; CHROMATIN; CELLS; LIGHT;
D O I
10.1038/nbt.4106
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The speed of super-resolution microscopy methods based on single-molecule localization, for example, PALM and STORM, is limited by the need to record many thousands of frames with a small number of observed molecules in each. Here, we present ANNA-PALM, a computational strategy that uses artificial neural networks to reconstruct super-resolution views from sparse, rapidly acquired localization images and/or widefield images. Simulations and experimental imaging of microtubules, nuclear pores, and mitochondria show that high-quality, super-resolution images can be reconstructed from up to two orders of magnitude fewer frames than usually needed, without compromising spatial resolution. Super-resolution reconstructions are even possible from widefield images alone, though adding localization data improves image quality. We demonstrate super-resolution imaging of >1,000 fields of view containing >1,000 cells in similar to 3 h, yielding an image spanning spatial scales from similar to 20 nm to similar to 2 mm. The drastic reduction in acquisition time and sample irradiation afforded by ANNA-PALM enables faster and gentler high-throughput and live-cell super-resolution imaging.
引用
收藏
页码:460 / +
页数:13
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