Literature DB >> 19453186

Quantum dot triexciton imaging with three-dimensional subdiffraction resolution.

Simon Hennig1, Sebastian van de Linde, Mike Heilemann, Markus Sauer.   

Abstract

We describe a simple method that improves optical resolution in fluorescence microscopy approximately 1.7-fold in all three dimensions and can be implemented on any basic confocal scanning microscope. This approach is based on three-photon absorption of commercially available quantum dots generating a triple exciton (triexciton) and subsequent blue-shifted fluorescence emission following recombination of the triexciton. As a pure physical approach, the resolution enhancement is independent from the nanoenvironment and demonstrated to work in living cells.

Year:  2009        PMID: 19453186     DOI: 10.1021/nl9012387

Source DB:  PubMed          Journal:  Nano Lett        ISSN: 1530-6984            Impact factor:   11.189


  4 in total

Review 1.  Fluorescence lifetime measurements and biological imaging.

Authors:  Mikhail Y Berezin; Samuel Achilefu
Journal:  Chem Rev       Date:  2010-05-12       Impact factor: 60.622

2.  Achieving increased resolution and more pixels with Superresolution Optical Fluctuation Imaging (SOFI).

Authors:  Thomas Dertinger; Ryan Colyer; Robert Vogel; Jörg Enderlein; Shimon Weiss
Journal:  Opt Express       Date:  2010-08-30       Impact factor: 3.894

3.  Simple method for sub-diffraction resolution imaging of cellular structures on standard confocal microscopes by three-photon absorption of quantum dots.

Authors:  Anje Sporbert; Zoltan Cseresnyes; Meike Heidbreder; Petra Domaing; Stefan Hauser; Barbara Kaltschmidt; Christian Kaltschmidt; Mike Heilemann; Darius Widera
Journal:  PLoS One       Date:  2013-05-21       Impact factor: 3.240

4.  Improvement of image resolution by combining enhanced confocal microscopy and quantum dot triexciton imaging.

Authors:  Simon Hennig; Dietmar J Manstein
Journal:  FEBS Open Bio       Date:  2021-07-26       Impact factor: 2.693

  4 in total

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