Literature DB >> 19118681

Chapter 12: Nanoscale biological fluorescence imaging: breaking the diffraction barrier.

Travis J Gould1, Samuel T Hess.   

Abstract

Biological imaging has been limited by the finite resolution of light microscopy. Recent developments in ultra-high-resolution microscopy methods, many of which are based on fluorescence, are breaking the diffraction barrier; it is becoming possible to image intracellular protein distributions with resolution of tens of nanometers or better. Fluorescence photoactivation localization microscopy (FPALM) is an example of such an ultra-high-resolution method which can image living or fixed cells with demonstrated lateral resolution of better than 20 nm. A detailed description of the methods involved in FPALM imaging of biological samples is presented here, accompanied by comparison with existing methods from the literature.

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Year:  2008        PMID: 19118681     DOI: 10.1016/S0091-679X(08)00612-2

Source DB:  PubMed          Journal:  Methods Cell Biol        ISSN: 0091-679X            Impact factor:   1.441


  8 in total

1.  Simultaneous multicolor imaging of biological structures with fluorescence photoactivation localization microscopy.

Authors:  Nikki M Curthoys; Michael J Mlodzianoski; Dahan Kim; Samuel T Hess
Journal:  J Vis Exp       Date:  2013-12-09       Impact factor: 1.355

Review 2.  Applying superresolution localization-based microscopy to neurons.

Authors:  Haining Zhong
Journal:  Synapse       Date:  2015-02-28       Impact factor: 2.562

Review 3.  Subdiffractive microscopy: techniques, applications, and challenges.

Authors:  Brian R Long; Danielle C Robinson; Haining Zhong
Journal:  Wiley Interdiscip Rev Syst Biol Med       Date:  2014-01-17

4.  The Role of Probe Photophysics in Localization-Based Superresolution Microscopy.

Authors:  Francesca Pennacchietti; Travis J Gould; Samuel T Hess
Journal:  Biophys J       Date:  2017-11-07       Impact factor: 4.033

5.  Model of bleaching and acquisition for superresolution microscopy controlled by a single wavelength.

Authors:  Alex Small
Journal:  Biomed Opt Express       Date:  2011-09-30       Impact factor: 3.732

Review 6.  Single-molecule fluorescence imaging: Generating insights into molecular interactions in virology.

Authors:  Sunaina Banerjee; Satyaghosh Maurya; Rahul Roy
Journal:  J Biosci       Date:  2018-07       Impact factor: 2.795

7.  Nanoscale imaging of caveolin-1 membrane domains in vivo.

Authors:  Kristin A Gabor; Dahan Kim; Carol H Kim; Samuel T Hess
Journal:  PLoS One       Date:  2015-02-03       Impact factor: 3.240

Review 8.  Super-resolution optical microscopy for studying membrane structure and dynamics.

Authors:  Erdinc Sezgin
Journal:  J Phys Condens Matter       Date:  2017-05-08       Impact factor: 2.333

  8 in total

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