Literature DB >> 23086874

Photoswitchable fluorophores for single-molecule localization microscopy.

Kieran Finan1, Benjamin Flottmann, Mike Heilemann.   

Abstract

Over the past decade, fluorescence microscopy has been revolutionized by the development of novel techniques that allow near-molecular resolution. Many such methods-collectively referred to as "single-molecule localization microscopy" (SMLM)-are based upon the repeated imaging of sparse stochastic subsets of the fluorophores in a sample. Active fluorophores are localized by finding the centers of their point spread functions, and a super-resolution image is constructed.Key to this strategy is the use of fluorophores that can be switched "on" and "off" in a controllable manner. Here we review the strengths and weaknesses of the wide variety of SMLM-compatible photoswitchable fluorophores and labeling strategies currently available. We also discuss their suitability for live-cell and multicolor imaging, as well as molecular counting.

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Year:  2013        PMID: 23086874     DOI: 10.1007/978-1-62703-137-0_9

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  Effect of Labeling Density and Time Post Labeling on Quality of Antibody-Based Super Resolution Microscopy Images.

Authors:  Amy M Bittel; Isaac Saldivar; Nicholas Dolman; Andrew Nickerson; Li-Jung Lin; Xiaolin Nan; Summer L Gibbs
Journal:  Proc SPIE Int Soc Opt Eng       Date:  2015-03-09
  1 in total

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