Tomographic STED microscopy.


Journal

Biomedical optics express
ISSN: 2156-7085
Titre abrégé: Biomed Opt Express
Pays: United States
ID NLM: 101540630

Informations de publication

Date de publication:
01 Jun 2020
Historique:
received: 02 03 2020
revised: 29 04 2020
accepted: 04 05 2020
entrez: 9 7 2020
pubmed: 9 7 2020
medline: 9 7 2020
Statut: epublish

Résumé

Stimulated emission depletion (STED) microscopy is a versatile imaging method with diffraction-unlimited resolution. Here, we present a novel STED microscopy variant that achieves either increased resolution at equal laser power or identical super-resolution conditions at significantly lower laser power when compared to the classical implementation. By applying a one-dimensional depletion pattern instead of the well-known doughnut-shaped STED focus, a more efficient depletion is achieved, thereby necessitating less STED laser power to achieve identical resolution. A two-dimensional resolution increase is obtained by recording a sequence of images with different high-resolution directions. This corresponds to a collection of tomographic projections within diffraction-limited spots, an approach that so far has not been explored in super-resolution microscopy. Via appropriate reconstruction algorithms, our method also provides an opportunity to speed up the acquisition process. Both aspects, the necessity of less STED laser power and the feasibility to decrease the recording time, have the potential to reduce photo-bleaching as well as sample damage drastically.

Identifiants

pubmed: 32637247
doi: 10.1364/BOE.391787
pii: 391787
pmc: PMC7316010
doi:

Types de publication

Journal Article

Langues

eng

Pagination

3139-3163

Informations de copyright

© 2020 Optical Society of America under the terms of the OSA Open Access Publishing Agreement.

Déclaration de conflit d'intérêts

JRK: Laser-Laboratory Göttingen e.V. (P), CG: Laser-Laboratory Göttingen e.V. (P), AE: Laser-Laboratory Göttingen e.V. (P), Abberior Instruments GmbH (I,C).

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Auteurs

Jennifer-Rose Krüger (JR)

Department of Optical Nanoscopy, Laser-Laboratory Göttingen e.V., Hans-Adolf-Krebs-Weg 1, D-37077 Göttingen, Germany.

Jan Keller-Findeisen (J)

Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, D-37077 Göttingen, Germany.

Claudia Geisler (C)

Department of Optical Nanoscopy, Laser-Laboratory Göttingen e.V., Hans-Adolf-Krebs-Weg 1, D-37077 Göttingen, Germany.

Alexander Egner (A)

Department of Optical Nanoscopy, Laser-Laboratory Göttingen e.V., Hans-Adolf-Krebs-Weg 1, D-37077 Göttingen, Germany.
Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells" (MBExC), University of Göttingen, Germany.

Classifications MeSH