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Projekt Druckansicht

STED Konfokalmikroskop

Fachliche Zuordnung Grundlagen der Biologie und Medizin
Förderung Förderung in 2008
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 70427742
 
Erstellungsjahr 2012

Zusammenfassung der Projektergebnisse

AG Stephan Sigrist (Fouquet, Andlauer): The majority of rapid cell-to-cell communication mechanisms and information processing within the nervous system makes use of chemical synapses. Thereby, the molecular organization of presynaptic active zones, the places where neurotransmitter filled synaptic vesicles get released, is a focus of intense investigation. We recently showed that Bruchpilot (BRP) of Drosophila melanogaster, which features homologies to the mammalian CAST/ERC family, is essential for structural organization and efficient neurotransmitter release at active zones. The light microscopic inspection of synaptic organization is often restricted by the limited resolution of conventional light microcopy due to diffraction. Thus, we stimulated emission depletion microscopy, STED for the analysis of synapse substructures. STED breaks the diffraction barrier and allows localization of proteins well below 100 nm. Using STED, we showed that BRP shapes the presynaptic active zone architecture by adopting an extended conformation, shining first light on the underlying macromolecular organization of active zones. AG Nieswandt (Gupta): STED analysis of the platelet cytoskeleton using different transgenic mouse models to study dynamics, subcellular localization of different signaling molecules and actin cytoskeleton in spreading platelets. AG Harms (Friedrich): Here, STED was combined with selective plane illumination microscopy (SPIM). Using this method, an up to 60% improvements in axial resolution with lateral resolution enhancements in control samples and zebrafish embryos coudl be reached. The integrated STED-SPIM method combines the advantages of SPIM with the resolution enhancement of STED, and thus provides a method for fast, high-resolution imaging with >100 µm deep penetration into biological tissue.

Projektbezogene Publikationen (Auswahl)

 
 

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