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      Multicolor Super-Resolution Imaging with Photo-Switchable Fluorescent Probes

      1 , 2 , 3 , 4 , 5 , 1 , 2 , 3 , 4 , 5 , 1 , 2 , 3 , 4 , 5 , 1 , 2 , 3 , 4 , 5
      Science
      American Association for the Advancement of Science (AAAS)

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          Abstract

          Recent advances in far-field optical nanoscopy have enabled fluorescence imaging with a spatial resolution of 20 to 50 nanometers. Multicolor super-resolution imaging, however, remains a challenging task. Here, we introduce a family of photo-switchable fluorescent probes and demonstrate multicolor stochastic optical reconstruction microscopy (STORM). Each probe consists of a photo-switchable “reporter” fluorophore that can be cycled between fluorescent and dark states, and an “activator” that facilitates photo-activation of the reporter. Combinatorial pairing of reporters and activators allows the creation of probes with many distinct colors. Iterative, color-specific activation of sparse subsets of these probes allows their localization with nanometer accuracy, enabling the construction of a super-resolution STORM image. Using this approach, we demonstrate multicolor imaging of DNA model samples and mammalian cells with 20- to 30-nanometer resolution. This technique will facilitate direct visualization of molecular interactions at the nanometer scale.

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          Most cited references30

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          Imaging intracellular fluorescent proteins at nanometer resolution.

          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.
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            Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM).

            We have developed a high-resolution fluorescence microscopy method based on high-accuracy localization of photoswitchable fluorophores. In each imaging cycle, only a fraction of the fluorophores were turned on, allowing their positions to be determined with nanometer accuracy. The fluorophore positions obtained from a series of imaging cycles were used to reconstruct the overall image. We demonstrated an imaging resolution of 20 nm. This technique can, in principle, reach molecular-scale resolution.
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              Far-field optical nanoscopy.

              In 1873, Ernst Abbe discovered what was to become a well-known paradigm: the inability of a lens-based optical microscope to discern details that are closer together than half of the wavelength of light. However, for its most popular imaging mode, fluorescence microscopy, the diffraction barrier is crumbling. Here, I discuss the physical concepts that have pushed fluorescence microscopy to the nanoscale, once the prerogative of electron and scanning probe microscopes. Initial applications indicate that emergent far-field optical nanoscopy will have a strong impact in the life sciences and in other areas benefiting from nanoscale visualization.
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                Author and article information

                Journal
                Science
                Science
                American Association for the Advancement of Science (AAAS)
                0036-8075
                1095-9203
                September 21 2007
                September 21 2007
                : 317
                : 5845
                : 1749-1753
                Affiliations
                [1 ]School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
                [2 ]Howard Hughes Medical Institute, Harvard University, Cambridge, MA 02138, USA.
                [3 ]Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA.
                [4 ]Graduate Program in Biophysics, Harvard University, Cambridge, MA 02138, USA.
                [5 ]Department of Physics, Harvard University, Cambridge, MA 02138, USA.
                Article
                10.1126/science.1146598
                2633025
                17702910
                fc84ad67-aeda-4ab9-b146-83d89727c1a7
                © 2007
                History

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