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Anwendung der Fluoreszenz-Korrelations-Spektroskopie zur Untersuchung dynamischer Prozesse in lebenden Zellen

dc.contributor.advisorNeher, Erwin Prof. Dr.de
dc.contributor.authorJordan, Randolfde
dc.date.accessioned2001-05-09T15:06:58Zde
dc.date.accessioned2013-01-18T10:35:38Zde
dc.date.available2013-01-30T23:51:05Zde
dc.date.issued2001-05-09de
dc.identifier.urihttp://hdl.handle.net/11858/00-1735-0000-0006-AE88-1de
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-2112
dc.format.mimetypeContentType:application/pdf Size:4966de
dc.language.isogerde
dc.rights.urihttp://webdoc.sub.gwdg.de/diss/copyrdiss.htmde
dc.titleAnwendung der Fluoreszenz-Korrelations-Spektroskopie zur Untersuchung dynamischer Prozesse in lebenden Zellende
dc.typedoctoralThesisde
dc.title.translatedApplication of fluorescence correlation spectroscopy to investigate dynamic processes in living cellsde
dc.contributor.refereeTroe, Jürgen Prof. Dr.de
dc.date.examination2000-10-31de
dc.subject.dnb540 Chemiede
dc.description.abstractengIn this thesis the Fluorescence Correlation Spectroscopy (FCS) technique is applied to cell-physiologically relevant reaction and diffusion problems in living cells. In the nucleus as well as in the cytoplasm of bovine adrenal chromaffin cells the FCS method is used to determine diffusion coefficients of calcium chelators that are often used as calcium indicators. At the interface of hippocampal cell membrane and extracellular solution the specific molecular interaction of a dye-labelled benzodiazepine with its receptor is examined. The affinity of the ligand-receptor-complex as well as the reaction rates of the complex are determined. The applicability of different dyes for ligand-labelling in FCS experiments is investigated. The FCS technique is suited to resolve the dynamics of single synaptic vesicles in hippocampal nerve endings. The effect of kinases, phosphatases and the cytoskeleton on the vesicle mobility are investigated. The mobility of these vesicles in unstimulated boutons is mainly due to active transport and under the control of the myosin light chain kinase. Inhibition of the phosphatases 1 and 2A leads to an increased vesicle mobility which can be further increased by destruction of the actin filaments in the synapse.de
dc.contributor.coRefereeZeeck, Axel Prof. Dr.de
dc.subject.topicMathematics and Computer Sciencede
dc.subject.engfluorescence correlation spectroscopyde
dc.subject.enghippocampal neuronde
dc.subject.engsynaptic vesiclede
dc.subject.engsynapsede
dc.subject.engbenzodiazepinede
dc.subject.engreceptor binding studyde
dc.subject.engdiffusion coefficientde
dc.subject.bk35.22de
dc.identifier.urnurn:nbn:de:gbv:7-webdoc-1016-8de
dc.identifier.purlwebdoc-1016de
dc.affiliation.instituteFakultät für Chemiede
dc.subject.gokfullSDde
dc.identifier.ppn330817736


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