Literature DB >> 17212534

High-speed confocal fluorescence imaging with a novel line scanning microscope.

Ralf Wolleschensky1, Bernhard Zimmermann, Michael Kempe.   

Abstract

Research in the life sciences increasingly involves the investigation of fast dynamic processes at the cellular and subcellular level. It requires tools to image complex systems with high temporal resolution in three-dimensional space. For this task, we introduce the concept of a fast fluorescence line scanner providing image acquisition speeds in excess of 100 frames per second at 512 x 512 pixels. Because the system preserves the capability for optical sectioning of confocal systems, it allows us to observe processes with three-dimensional resolution. We describe the principle of operation, the optical characteristics of the microscope, and cover several applications in particular from the field of cell and developmental biology. A commercial system based on the line scanning concept has been realized by Carl Zeiss (LSM 5 LIVE).

Mesh:

Year:  2006        PMID: 17212534     DOI: 10.1117/1.2402110

Source DB:  PubMed          Journal:  J Biomed Opt        ISSN: 1083-3668            Impact factor:   3.170


  21 in total

1.  Line-scanning confocal microscopy for high-resolution imaging of upconverting rare-earth-based contrast agents.

Authors:  Laura M Higgins; Margot Zevon; Vidya Ganapathy; Yang Sheng; Mei Chee Tan; Richard E Riman; Charles M Roth; Prabhas V Moghe; Mark C Pierce
Journal:  J Biomed Opt       Date:  2015-11       Impact factor: 3.170

2.  Understanding biological dynamics: following cells and molecules to track functions and mechanisms.

Authors:  A Palamidessi; I Testa; E Frittoli; S Barozzi; M Garrè; D Mazza; P P Di Fiore; A Diaspro; G Scita; Mario Faretta
Journal:  Eur Biophys J       Date:  2009-05-20       Impact factor: 1.733

3.  Fast fluorescence microscopy for imaging the dynamics of embryonic development.

Authors:  Julien Vermot; Scott E Fraser; Michael Liebling
Journal:  HFSP J       Date:  2008-05-13

4.  Cylindrical illumination confocal spectroscopy: rectifying the limitations of confocal single molecule spectroscopy through one-dimensional beam shaping.

Authors:  Kelvin J Liu; Tza-Huei Wang
Journal:  Biophys J       Date:  2008-05-30       Impact factor: 4.033

5.  High-speed multicolor microscopy of repeating dynamic processes.

Authors:  Jungho Ohn; Jennifer Yang; Scott E Fraser; Rusty Lansford; Michael Liebling
Journal:  Genesis       Date:  2011-06-21       Impact factor: 2.487

6.  Rapid imaging of large tissues using high-resolution stage-scanning microscopy.

Authors:  Tao Yang; Ting Zheng; Zhenhua Shang; Xiaojun Wang; Xiaohua Lv; Jing Yuan; Shaoqun Zeng
Journal:  Biomed Opt Express       Date:  2015-04-23       Impact factor: 3.732

7.  Direct comparison between confocal and multiphoton microscopy for rapid histopathological evaluation of unfixed human breast tissue.

Authors:  Tadayuki Yoshitake; Michael G Giacomelli; Lucas C Cahill; Daniel B Schmolze; Hilde Vardeh; Beverly E Faulkner-Jones; James L Connolly; James G Fujimoto
Journal:  J Biomed Opt       Date:  2016-12-01       Impact factor: 3.170

8.  Video-rate confocal microscopy for single-molecule imaging in live cells and superresolution fluorescence imaging.

Authors:  Jinwoo Lee; Yukihiro Miyanaga; Masahiro Ueda; Sungchul Hohng
Journal:  Biophys J       Date:  2012-10-16       Impact factor: 4.033

9.  Line-scanning reflectance confocal microscopy of human skin: comparison of full-pupil and divided-pupil configurations.

Authors:  Daniel S Gareau; Sanjee Abeytunge; Milind Rajadhyaksha
Journal:  Opt Lett       Date:  2009-10-15       Impact factor: 3.776

10.  Visualization of lipid raft membrane compartmentalization in living RN46A neuronal cells using single quantum dot tracking.

Authors:  Jerry C Chang; Sandra J Rosenthal
Journal:  ACS Chem Neurosci       Date:  2012-08-01       Impact factor: 4.418

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