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Scanning X-Ray Nanodiffraction on Dictyostelium discoideum

dc.contributor.advisorSalditt, Tim Prof. Dr.
dc.contributor.authorPriebe, Marius Patrick
dc.date.accessioned2015-11-06T10:25:48Z
dc.date.available2015-11-06T10:25:48Z
dc.date.issued2015-11-06
dc.identifier.urihttp://hdl.handle.net/11858/00-1735-0000-0023-967B-2
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-5183
dc.language.isoengde
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc530de
dc.titleScanning X-Ray Nanodiffraction on Dictyostelium discoideumde
dc.typedoctoralThesisde
dc.contributor.refereeSalditt, Tim Prof. Dr.
dc.date.examination2015-02-04
dc.subject.gokPhysik (PPN621336750)de
dc.description.abstractengIn the recent years, novel focussing optics for synchrotron radiation sources became available, which now allow focussing the x-radiation down to 100\,nm (FWHM). Thus, the typically poor spatial resolution of Small Angle X-ray Scattering (SAXS) has been overcome and enables "Scanning X-ray Nanodiffraction", where a sample is scanned in a linewise motion, while recording a far-field diffraction pattern at every scanning position. In this work, Scanning Nanodiffraction was applied to single cells of the amoeba \textit{Dictyostelium discoideum}, which is a model system for amoeboid migration, that is enabled by a reorganization of cytoskeletal biopolymers in the cell cortex. The spatially resolved small angle x-ray diffraction signal shows characteristic streak-like patterns in reciprocal space, which is attributed to fibre bundles of the actomyosin network. An anisotropy parameter nicknamed "Streak Finder" is introduced to characterize the pronounced local variations within the cell. The x-ray differential phase contrast is evaluated in terms of the projected electron density and additional x-ray fluorescence aquisitions provide information on the spatially resolved distribution (2D) of elements within the cell. The x-ray results are correlated with optical microscopy (phase contrast and fluorescence microscopy of strains with labelled actin and myosin II) on live, fixed, and cryogenic cells.de
dc.contributor.coRefereeEnderlein, Jörg Prof. Dr.
dc.contributor.thirdRefereeBodenschatz, Eberhard Prof. Dr.
dc.contributor.thirdRefereeKöster, Sarah Prof. Dr.
dc.contributor.thirdRefereeTechert, Simone Prof. Dr.
dc.contributor.thirdRefereeHub, Jochen S. Dr.
dc.subject.engNanodiffractionde
dc.subject.engDictyostelium discoideumde
dc.subject.engActinde
dc.subject.engMyosin-IIde
dc.subject.engStreak Finderde
dc.subject.engSAXSde
dc.subject.engSTXMde
dc.subject.engFluorescence mappingde
dc.subject.engPtychographyde
dc.subject.engX-rayde
dc.subject.engVitrificationde
dc.subject.engFrozen-hydrated cellsde
dc.subject.engSample preparationde
dc.identifier.urnurn:nbn:de:gbv:7-11858/00-1735-0000-0023-967B-2-9
dc.affiliation.instituteFakultät für Physikde
dc.identifier.ppn842309098


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