Literature DB >> 31565507

Correlative two-color two-photon (2C2P) excitation STED microscopy.

Christoph Polzer1,2, Stefan Ness3, Mojtaba Mohseni1, Thomas Kellerer1, Markus Hilleringmann3, Joachim Rädler2, Thomas Hellerer1.   

Abstract

We present a two-color two-photon stimulated emission depletion microscopy technique (2C2P-STED) that correlates a confocal image with a super-resolved image employing the inherent self-referencing mechanism of nonlinear excitation. The novel approach overcomes the substantial challenge posed by two different imaging modalities in laser-scanning fluorescence microscopy for colocalization on the nanometer scale. Demonstrating the principle of 2C2P-STED, we show for the first time super-resolved images of the gram-positive bacteria Streptococcus pneumoniae TIGR4 pilus type-1. A signal-to-noise ratio (SNR) greater than 10 was achieved in 2C2P excitation mode and approximately 70 nm details were resolved in 2P-STED.
© 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement.

Entities:  

Year:  2019        PMID: 31565507      PMCID: PMC6757464          DOI: 10.1364/BOE.10.004516

Source DB:  PubMed          Journal:  Biomed Opt Express        ISSN: 2156-7085            Impact factor:   3.732


  28 in total

Review 1.  Two-photon excitation fluorescence microscopy.

Authors:  P T So; C Y Dong; B R Masters; K M Berland
Journal:  Annu Rev Biomed Eng       Date:  2000       Impact factor: 9.590

2.  Breaking Abbe's diffraction resolution limit in fluorescence microscopy with stimulated emission depletion beams of various shapes.

Authors:  T A Klar; E Engel; S W Hell
Journal:  Phys Rev E Stat Nonlin Soft Matter Phys       Date:  2001-11-26

3.  Single-wavelength two-photon excitation-stimulated emission depletion (SW2PE-STED) superresolution imaging.

Authors:  Paolo Bianchini; Benjamin Harke; Silvia Galiani; Giuseppe Vicidomini; Alberto Diaspro
Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-09       Impact factor: 11.205

Review 4.  Deep tissue two-photon microscopy.

Authors:  Fritjof Helmchen; Winfried Denk
Journal:  Nat Methods       Date:  2005-12       Impact factor: 28.547

5.  Stimulated emission depletion microscopy with a supercontinuum source and fluorescence lifetime imaging.

Authors:  Egidijus Auksorius; Bosanta R Boruah; Christopher Dunsby; Peter M P Lanigan; Gordon Kennedy; Mark A A Neil; Paul M W French
Journal:  Opt Lett       Date:  2008-01-15       Impact factor: 3.776

6.  Efficient fluorescence inhibition patterns for RESOLFT microscopy.

Authors:  Jan Keller; Andreas Schönle; Stefan W Hell
Journal:  Opt Express       Date:  2007-03-19       Impact factor: 3.894

7.  Two-color two-photon excitation of fluorescence.

Authors:  J R Lakowicz; I Gryczynski; H Malak; Z Gryczynski
Journal:  Photochem Photobiol       Date:  1996-10       Impact factor: 3.421

8.  Two-photon laser scanning fluorescence microscopy.

Authors:  W Denk; J H Strickler; W W Webb
Journal:  Science       Date:  1990-04-06       Impact factor: 47.728

9.  The power of correlative microscopy: multi-modal, multi-scale, multi-dimensional.

Authors:  Jeffrey Caplan; Marc Niethammer; Russell M Taylor; Kirk J Czymmek
Journal:  Curr Opin Struct Biol       Date:  2011-07-21       Impact factor: 6.809

10.  Sortase-mediated assembly and surface topology of adhesive pneumococcal pili.

Authors:  Stefan Fälker; Aaron L Nelson; Eva Morfeldt; Kristina Jonas; Kjell Hultenby; Johannes Ries; Ojar Melefors; Staffan Normark; Birgitta Henriques-Normark
Journal:  Mol Microbiol       Date:  2008-09-17       Impact factor: 3.501

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