| Literature DB >> 23086874 |
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.Mesh:
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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