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search.filters.applied.f.access: openAccess × End date: 2019 × Start date: 2019 × End date: 2015 × Start date: 2012 × Type: Text × Publisher: London : Nature Publishing Group × WGL Institute: INM ×

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    X-ray imaging with scintillator-sensitized hybrid organic photodetectors
    (London : Nature Publishing Group, 2015) Büchele, Patric; Richter, Moses; Tedde, Sandro F.; Matt, Gebhard J.; Ankah, Genesis N.; Fischer, Rene; Biele, Markus; Metzger, Wilhelm; Lilliu, Samuele; Bikondoa, Oier; Macdonald, J. Emyr; Brabec, Christoph J.; Kraus, Tobias; Lemmer, Uli; Schmidt, Oliver
    Medical X-ray imaging requires cost-effective and high-resolution flat-panel detectors for the energy range between 20 and 120 keV. Solution-processed photodetectors provide the opportunity to fabricate detectors with a large active area at low cost. Here, we present a disruptive approach that improves the resolution of such detectors by incorporating terbium-doped gadolinium oxysulfide scintillator particles into an organic photodetector matrix. The X-ray induced light emission from the scintillators is absorbed within hundreds of nanometres, which is negligible compared with the pixel size. Hence, optical crosstalk, a limiting factor in the resolution of scintillator-based X-ray detectors, is minimized. The concept is validated with a 256 × 256 pixel detector with a resolution of 4.75 lp mm−1 at a MTF = 0.2, significantly better than previous stacked scintillator-based flat-panel detectors. We achieved a resolution that proves the feasibility of solution-based detectors in medical applications. Time-resolved electrical characterization showed enhanced charge carrier mobility with increased scintillator filling, which is explained by morphological changes.
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    Lipid droplets as a novel cargo of tunnelling nanotubes in endothelial cells
    (London : Nature Publishing Group, 2015) Astanina, Ksenia; Koch, Marcus; Jüngst, Christian; Zumbusch, Andreas; Kiemer, Alexandra K.
    Intercellular communication is a fundamental process in the development and functioning of multicellular organisms. Recently, an essentially new type of intercellular communication, based on thin membrane channels between cells, has been reported. These structures, termed intercellular or tunnelling nanotubes (TNTs), permit the direct exchange of various components or signals (e.g., ions, proteins, or organelles) between non-adjacent cells at distances over 100 μm. Our studies revealed the presence of tunnelling nanotubes in microvascular endothelial cells (HMEC-1). The TNTs were studied with live cell imaging, environmental scanning electron microscopy (ESEM), and coherent anti-Stokes Raman scattering spectroscopy (CARS). Tunneling nanotubes showed marked persistence: the TNTs could connect cells over long distances (up to 150 μm) for several hours. Several cellular organelles were present in TNTs, such as lysosomes and mitochondria. Moreover, we could identify lipid droplets as a novel type of cargo in the TNTs. Under angiogenic conditions (VEGF treatment) the number of lipid droplets increased significantly. Arachidonic acid application not only increased the number of lipid droplets but also tripled the extent of TNT formation. Taken together, our results provide the first demonstration of lipid droplets as a cargo of TNTs and thereby open a new field in intercellular communication research.
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    Epidermal growth factor receptor subunit locations determined in hydrated cells with environmental scanning electron microscopy
    (London : Nature Publishing Group, 2013) Peckys, Diana B; Baudoin, Jean-Pierre; Eder, Magdalena; Werner, Ulf; de Jonge, Niels
    Imaging single epidermal growth factor receptors (EGFR) in intact cells is presently limited by the available microscopy methods. Environmental scanning electron microscopy (ESEM) of whole cells in hydrated state in combination with specific labeling with gold nanoparticles was used to localize activated EGFRs in the plasma membranes of COS7 and A549 cells. The use of a scanning transmission electron microscopy (STEM) detector yielded a spatial resolution of 3 nm, sufficient to identify the locations of individual EGFR dimer subunits. The sizes and distribution of dimers and higher order clusters of EGFRs were determined. The distance between labels bound to dimers amounted to 19 nm, consistent with a molecular model. A fraction of the EGFRs was found in higher order clusters with sizes ranging from 32–56 nm. ESEM can be used for quantitative whole cell screening studies of membrane receptors, and for the study of nanoparticle-cell interactions in general.