DNA and chromatin imaging with super-resolution fluorescence microscopy based on single-molecule localization |
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Authors: | Flors Cristina |
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Affiliation: | School of Chemistry and Collaborative Optical Spectroscopy, Micromanipulation and Imaging Center (COSMIC), University of Edinburgh, Joseph Black Building, The King's Buildings, West Mains Road, EH9 3JJ Edinburgh, UK. cristina.flors@ed.ac.uk |
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Abstract: | With the expansion of super-resolution fluorescence microscopy methods, it is now possible to access the organization of cells and materials at the nanoscale by optical means. This review discusses recent progress in super-resolution imaging of isolated and cell DNA using single-molecule localization methods. A high labeling density of photoswitchable fluorophores is crucial for these techniques, which can be provided by sequence independent DNA stains in which photoblinking reactions can be induced. In particular, unsymmetrical cyanine intercalating dyes in combination with special buffers can be used to image isolated DNA with a spatial resolution of 30-40 nm. For super-resolution imaging of chromatin, cell permeant cyanine dyes that bind the minor groove of DNA have the potential to become a useful alternative to the labeling of histones and other DNA-associated proteins. Other recent developments that are interesting in this context such as high density labeling methods or new DNA probes with photoswitching functionalities are also surveyed. Progress in labeling, optics, and single-molecule localization algorithms is being rapid, and it is likely to provide real insight into DNA structuring in cells and materials. |
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