Literature DB >> 20173926

Birefringent device converts a standard scanning microscope into a STED microscope that also maps molecular orientation.

Matthias Reuss1, Johann Engelhardt, Stefan W Hell.   

Abstract

Stimulated emission depletion (STED) microscopy usually employs a scanning excitation beam that is superimposed by a donut-shaped STED beam for keeping the fluorophores at the periphery of the excitation spot dark. Here, we introduce a simple birefringent device that produces a donut-shaped focal spot with suitable polarization for STED, while leaving the excitation spot virtually intact. The device instantly converts a scanning (confocal) microscope with a co-aligned STED beam into a full-blown STED microscope. The donut can be adapted to reveal, through the resulting fluorescence image, the orientation of fluorophores in the sample, thus directly providing subdiffraction resolution images of molecular orientation.

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Year:  2010        PMID: 20173926     DOI: 10.1364/OE.18.001049

Source DB:  PubMed          Journal:  Opt Express        ISSN: 1094-4087            Impact factor:   3.894


  11 in total

1.  Ultrafast, temporally stochastic STED nanoscopy of millisecond dynamics.

Authors:  Jale Schneider; Jasmin Zahn; Marta Maglione; Stephan J Sigrist; Jonas Marquard; Jakub Chojnacki; Hans-Georg Kräusslich; Steffen J Sahl; Johann Engelhardt; Stefan W Hell
Journal:  Nat Methods       Date:  2015-07-27       Impact factor: 28.547

Review 2.  Optical imaging of nanoscale cellular structures.

Authors:  Per Niklas Hedde; Gerd Ulrich Nienhaus
Journal:  Biophys Rev       Date:  2010-09-08

3.  Improved optical slicing by stimulated emission depletion light sheet microscopy.

Authors:  José Martínez Hernández; Alain Buisson; Irène Wang; Jean-Claude Vial
Journal:  Biomed Opt Express       Date:  2020-01-08       Impact factor: 3.732

4.  STED super-resolved microscopy.

Authors:  Giuseppe Vicidomini; Paolo Bianchini; Alberto Diaspro
Journal:  Nat Methods       Date:  2018-01-29       Impact factor: 28.547

Review 5.  Fluorescence microscopy.

Authors:  Michael J Sanderson; Ian Smith; Ian Parker; Martin D Bootman
Journal:  Cold Spring Harb Protoc       Date:  2014-10-01

6.  Differential localization of SAP102 and PSD-95 is revealed in hippocampal spines using super-resolution light microscopy.

Authors:  Chan-Ying Zheng; Ya-Xia Wang; Bechara Kachar; Ronald S Petralia
Journal:  Commun Integr Biol       Date:  2011-01

7.  Upgrade of a Scanning Confocal Microscope to a Single-Beam Path STED Microscope.

Authors:  André Klauss; Marcelle König; Carsten Hille
Journal:  PLoS One       Date:  2015-06-19       Impact factor: 3.240

8.  Nanoscopic spine localization of Norbin, an mGluR5 accessory protein.

Authors:  Linda Westin; Matthias Reuss; Maria Lindskog; Anita Aperia; Hjalmar Brismar
Journal:  BMC Neurosci       Date:  2014-03-26       Impact factor: 3.288

9.  Correlative microscopy approach for biology using X-ray holography, X-ray scanning diffraction and STED microscopy.

Authors:  M Bernhardt; J-D Nicolas; M Osterhoff; H Mittelstädt; M Reuss; B Harke; A Wittmeier; M Sprung; S Köster; T Salditt
Journal:  Nat Commun       Date:  2018-09-07       Impact factor: 14.919

10.  Advanced easySTED microscopy based on two-photon excitation by electrical modulations of light pulse wavefronts.

Authors:  Kohei Otomo; Terumasa Hibi; Yi-Cheng Fang; Jui-Hung Hung; Motosuke Tsutsumi; Ryosuke Kawakami; Hiroyuki Yokoyama; Tomomi Nemoto
Journal:  Biomed Opt Express       Date:  2018-05-15       Impact factor: 3.732

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