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Imaging label-free intracellular structures by localisation microscopy

期刊

MICRON
卷 42, 期 4, 页码 348-352

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.micron.2010.03.006

关键词

Sub-diffraction limit microscopy; Localisation microscopy; Spectral Precision Distance Microscopy (SPDM); Fluorescence

资金

  1. University Heidelberg
  2. Deutsche Forschungsgemeinschaft [SPP1128]
  3. European Union
  4. Federal Ministry of Education and Research (BMBF)

向作者/读者索取更多资源

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 lambda/10 range (similar to 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. (C) 2010 Elsevier Ltd. All rights reserved.

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