Literature DB >> 15817377

Fluorescence microscopy with super-resolved optical sections.

Alexander Egner1, Stefan W Hell.   

Abstract

The fluorescence microscope, especially its confocal variant, has become a standard tool in cell biology research for delivering 3D-images of intact cells. However, the resolution of any standard optical microscope is at least 3 times poorer along the axis of the lens that in its focal plane. Here, we review principles and applications of an emerging family of fluorescence microscopes, such as 4Pi microscopes, which improve axial resolution by a factor of seven by employing two opposing lenses. Noninvasive axial sections of 80-160 nm thickness deliver more faithful 3D-images of subcellular features, providing a new opportunity to significantly enhance our understanding of cellular structure and function.

Mesh:

Year:  2005        PMID: 15817377     DOI: 10.1016/j.tcb.2005.02.003

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  20 in total

1.  [Super-resolution optical microscopy of the organ of Corti. Investigations on the fine structure of the inner hair cell afferent synapse by the 4Pi and STED techniques].

Authors:  A C Meyer; D Khimich; A Egner; T Moser
Journal:  HNO       Date:  2012-08       Impact factor: 1.284

2.  Ultra-high resolution imaging by fluorescence photoactivation localization microscopy.

Authors:  Samuel T Hess; Thanu P K Girirajan; Michael D Mason
Journal:  Biophys J       Date:  2006-09-15       Impact factor: 4.033

3.  Two-photon excitation and photoconversion of EosFP in dual-color 4Pi confocal microscopy.

Authors:  Sergey Ivanchenko; Sylvia Glaschick; Carlheinz Röcker; Franz Oswald; Jörg Wiedenmann; G Ulrich Nienhaus
Journal:  Biophys J       Date:  2007-03-23       Impact factor: 4.033

4.  Differential evanescence nanometry: live-cell fluorescence measurements with 10-nm axial resolution on the plasma membrane.

Authors:  Saveez Saffarian; Tomas Kirchhausen
Journal:  Biophys J       Date:  2007-11-09       Impact factor: 4.033

Review 5.  Single-molecule biophysics: at the interface of biology, physics and chemistry.

Authors:  Ashok A Deniz; Samrat Mukhopadhyay; Edward A Lemke
Journal:  J R Soc Interface       Date:  2008-01-06       Impact factor: 4.118

6.  Three-dimensional super-resolution imaging by stochastic optical reconstruction microscopy.

Authors:  Bo Huang; Wenqin Wang; Mark Bates; Xiaowei Zhuang
Journal:  Science       Date:  2008-01-03       Impact factor: 47.728

7.  Microscopy and its focal switch.

Authors:  Stefan W Hell
Journal:  Nat Methods       Date:  2009-01       Impact factor: 28.547

8.  Axial resolution enhancement by 4Pi confocal fluorescence microscopy with two-photon excitation.

Authors:  Sylvia Glaschick; Carlheinz Röcker; Karen Deuschle; Jörg Wiedenmann; Franz Oswald; Volker Mailänder; G Ulrich Nienhaus
Journal:  J Biol Phys       Date:  2008-06-19       Impact factor: 1.365

9.  4Pi microscopy of the nuclear pore complex.

Authors:  Jana Hüve; Ramona Wesselmann; Martin Kahms; Reiner Peters
Journal:  Biophys J       Date:  2008-03-28       Impact factor: 4.033

10.  Adenosine modulates transmission at the hippocampal mossy fibre synapse via direct inhibition of presynaptic calcium channels.

Authors:  A Gundlfinger; J Bischofberger; F W Johenning; M Torvinen; D Schmitz; J Breustedt
Journal:  J Physiol       Date:  2007-05-03       Impact factor: 5.182

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