| Literature DB >> 20538472 |
Rainer Kaufmann1, Patrick Müller2, Michael Hausmann2, Christoph Cremer3.
Abstract
Localisation microscopy methods allow to realize a light optical resolution far beyond the Abbe-Rayleigh limit of about 200 nm laterally and 600 nm axially. So far, this progress was achieved using labelling with appropriate fluorochromes and fluorescent proteins. Here, we describe for the first time that optical resolution of cellular structures in the λ/10 range (∼50 nm) can be achieved even in label-free cells. This was obtained using Spectral Precision Distance/Position Determination Microscopy (SPDM), a method based on the general principles of localisation microscopy. Besides a substantial resolution improvement of autofluorescent structures, SPDM revealed cellular objects which are not detectable under conventional fluorescence imaging conditions.Mesh:
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Year: 2010 PMID: 20538472 DOI: 10.1016/j.micron.2010.03.006
Source DB: PubMed Journal: Micron ISSN: 0968-4328 Impact factor: 2.251