Deep learning enables fast, gentle STED microscopy

Vahid Ebrahimi, Till Stephan, Jiah Kim, Pablo Carravilla, Christian Eggeling, Stefan Jakobs, Kyu Young Han

Communications Biology 2023 article cited by 44

importance 4/10 solved Advanced Fluorescence Microscopy Techniques microscopy / cell imaging stage: research

STED super-resolution microscopy damages and bleaches samples because of long pixel dwell times, limiting live-cell imaging.

Photodamage restricts how long scientists can image dynamic subcellular processes such as mitochondrial movement.

A deep learning method denoises STED images, allowing pixel dwell time to be cut by one or two orders of magnitude while restoring noisy 2D and 3D images.

Pixel dwell time reduced by one or two orders of magnitude; robust restoration of noisy 2D and 3D STED images; long-term imaging of mitochondrial dynamics.

Enables gentler, longer-term super-resolution imaging of live subcellular structures.

Venue Communications Biology
Published 2023
Work type article
Authors Vahid Ebrahimi, Till Stephan, Jiah Kim, Pablo Carravilla, Christian Eggeling, Stefan Jakobs, Kyu Young Han
Citations 44 (OpenAlex, at import time)
References 40
Model or method not stated in source
Organization not stated in source
Primary source https://doi.org/10.1038/s42003-023-05054-z
Open access gold
Keywords STED microscopy, deep learning, denoising, photobleaching, super-resolution, mitochondrial dynamics
4 / 10

real but narrower advance

Photodamage limits live-cell super-resolution imaging, a real but narrow methodological advance benefiting microscopy researchers; abstract gives no scale of broader impact.

Basis: inferred. Judged from the source text, which gives no explicit scale. Stated scale: not stated in source. Method and limits.

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