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      X-ray ptychographic and fluorescence microscopy of frozen-hydrated cells using continuous scanning

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          Abstract

          X-ray microscopy can be used to image whole, unsectioned cells in their native hydrated state. It complements the higher resolution of electron microscopy for submicrometer thick specimens, and the molecule-specific imaging capabilites of fluorescence light microscopy. We describe here the first use of fast, continuous x-ray scanning of frozen hydrated cells for simultaneous sub-20 nm resolution ptychographic transmission imaging with high contrast, and sub-100 nm resolution deconvolved x-ray fluorescence imaging of diffusible and bound ions at native concentrations, without the need to add specific labels. By working with cells that have been rapidly frozen without the use of chemical fixatives, and imaging them under cryogenic conditions, we are able to obtain images with well preserved structural and chemical composition, and sufficient stability against radiation damage to allow for multiple images to be obtained with no observable change.

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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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            Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy.

            Lateral resolution that exceeds the classical diffraction limit by a factor of two is achieved by using spatially structured illumination in a wide-field fluorescence microscope. The sample is illuminated with a series of excitation light patterns, which cause normally inaccessible high-resolution information to be encoded into the observed image. The recorded images are linearly processed to extract the new information and produce a reconstruction with twice the normal resolution. Unlike confocal microscopy, the resolution improvement is achieved with no need to discard any of the emission light. The method produces images of strikingly increased clarity compared to both conventional and confocal microscopes.
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              Extending the methodology of X-ray crystallography to allow imaging of micrometre-sized non-crystalline specimens

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                Author and article information

                Contributors
                cjacobsen@anl.gov
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                27 March 2017
                27 March 2017
                2017
                : 7
                : 445
                Affiliations
                [1 ]ISNI 0000 0001 2299 3507, GRID grid.16753.36, Applied Physics, , Northwestern University, ; Evanston, IL 60208 USA
                [2 ]ISNI 0000 0001 1939 4845, GRID grid.187073.a, Advanced Photon Source, , Argonne National Laboratory, ; Argonne, IL 60439 USA
                [3 ]ISNI 0000 0001 2299 3507, GRID grid.16753.36, Department of Physics & Astronomy, , Northwestern University, ; Evanston, IL 60208 USA
                [4 ]ISNI 0000 0001 1939 4845, GRID grid.187073.a, Mathematics and Computing Science Division, , Argonne National Laboratory, ; Argonne, IL 60439 USA
                [5 ]ISNI 0000 0001 2299 3507, GRID grid.16753.36, Chemistry of Life Processes Institute, , Northwestern University, ; Evanston, IL 60208 USA
                [6 ]ISNI 0000 0001 1939 4845, GRID grid.187073.a, X-ray Science Division, Advanced Photon Source, , Argonne National Laboratory, ; Argonne, IL 60439 USA
                [7 ]ISNI 0000 0001 2231 4551, GRID grid.184769.5, Advanced Light Source, , Lawrence Berkeley National Laboratory, ; Berkeley, CA 94720 USA
                Author information
                http://orcid.org/0000-0001-8562-0353
                Article
                569
                10.1038/s41598-017-00569-y
                5428657
                28348401
                67ce4fa8-1d50-4b6d-902d-382274dedfb7
                © The Author(s) 2017

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 25 October 2016
                : 3 March 2017
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