Imaging intracellular fluorescent proteins at nanometer resolution
- PMID: 16902090
 - DOI: 10.1126/science.1127344
 
Imaging intracellular fluorescent proteins at nanometer resolution
Abstract
We introduce a method for optically imaging intracellular proteins at nanometer spatial resolution. Numerous sparse subsets of photoactivatable fluorescent protein molecules were activated, localized (to approximately 2 to 25 nanometers), and then bleached. The aggregate position information from all subsets was then assembled into a superresolution image. We used this method--termed photoactivated localization microscopy--to image specific target proteins in thin sections of lysosomes and mitochondria; in fixed whole cells, we imaged vinculin at focal adhesions, actin within a lamellipodium, and the distribution of the retroviral protein Gag at the plasma membrane.
Comment in
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  The limits of light.Nat Rev Mol Cell Biol. 2010 Oct;11(10):678. doi: 10.1038/nrm2989. Nat Rev Mol Cell Biol. 2010. PMID: 20861874 No abstract available.
 
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