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Nat Biotechnol. 2018 Jun;36(5):460-468. doi: 10.1038/nbt.4106. Epub 2018 Apr 16.

Deep learning massively accelerates super-resolution localization microscopy.

Ouyang W1,2,3, Aristov A1,2,3, Lelek M1,2,3, Hao X1,2,3, Zimmer C1,2,3.

Author information

1
Institut Pasteur, Unité Imagerie et Modélisation, Paris, France.
2
UMR 3691, CNRS, Paris, France.
3
C3BI, USR 3756, IP CNRS, Paris, France.

Abstract

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 ∼3 h, yielding an image spanning spatial scales from ∼20 nm 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.

PMID:
29658943
DOI:
10.1038/nbt.4106
[Indexed for MEDLINE]

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