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Klonieren und Charakterisieren von P/Q-Typ-Calciumkanälen für Mikroskopie an lebenden Zellen

dc.contributor.advisorNeher, Erwin Prof. Dr.de
dc.contributor.authorJuha, Martinde
dc.date.accessioned2013-09-03T13:58:36Z
dc.date.available2013-09-13T22:50:04Z
dc.date.issued2013-09-03de
dc.identifier.urihttp://hdl.handle.net/11858/00-1735-0000-0001-BB49-0
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-4030
dc.language.isodeude
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/
dc.subject.ddc610de
dc.titleKlonieren und Charakterisieren von P/Q-Typ-Calciumkanälen für Mikroskopie an lebenden Zellende
dc.typedoctoralThesisde
dc.title.translatedCloning and characterization of P/Q-type calcium channels for live cell imagingde
dc.contributor.refereeWouters, Fred Prof. Dr.de
dc.date.examination2013-09-03de
dc.description.abstractengIn all excitable cells voltage-dependent calcium channels can be found. They mediate the entry of calcium into cells following depolarization. Calcium contributes to a wide variety of cellular response like muscle contraction, neurotransmitter release, gene expression and also synaptogenesis. For the neurotransmitter release vesicles are needed and the release is supported from a variety of different proteins. Research in the field of neurotransmitter release revealed the probable existence of two different vesicle populations within the RRP which differ in their release probability, the velocity of recruitment and their fusion competence. These different characteristics might be caused by a significant heterogeneity concerning the distance between the vesicle and the controlling calcium channels. To approximate these presumptions and to specify the exact location of P/Q-type calcium channels a specific labeling of the α1-subunit of these channels was performed. The labeling technique included the covalent labeling of the α1-subunit using a short 11- residue -long ACP-ybbR-Tag and an adenoviral expression system under the requirements of live cell imaging. Besides this, experiments using the STED-microscope were carried out. Although the specific labeling of P/Q-type calcium channels could neither be successfully performed in HEK293 cells, nor in hippocampal neurons nor by using the STED-microscope, it could be demonstrated that the ACP labeling procedure works in general using the chosen methods. A specific membrane labeling was performed. It could also be proven that the inserted tag did not disturb the function of the calcium channel.de
dc.contributor.coRefereeOppermann, Martin Prof. Dr.de
dc.subject.gerCalciumkanälede
dc.subject.gerVesikelpoolde
dc.subject.gerTransmitterfreisetzungde
dc.subject.gerCalciumkanal-bedingte Erkrankungende
dc.subject.gerFärbemethodende
dc.subject.gerschnell-freisetzende Vesikelde
dc.subject.gerlangsam-freisetzende Vesikelde
dc.subject.engcalcium channelsde
dc.subject.engvesicle poolde
dc.subject.engACP-labelingde
dc.subject.engybbRde
dc.subject.engtransmitter releasede
dc.subject.engSNAREde
dc.subject.engcalcium channelopathiesde
dc.subject.englabeling methodsde
dc.subject.engslow-releasing vesiclesde
dc.subject.engfast-releasing vesiclesde
dc.subject.engcalcium clusterde
dc.subject.englive cell imagingde
dc.identifier.urnurn:nbn:de:gbv:7-11858/00-1735-0000-0001-BB49-0-4
dc.affiliation.instituteMedizinische Fakultätde
dc.subject.gokfullPhysiologie / Pathophysiologie - Allgemein- und Gesamtdarstellungen (PPN619875283)de
dc.subject.gokfullMethoden und Techniken in der Medizin (PPN619875143)de
dc.subject.gokfullPhysik / Biopyhsik / Biomedizinische Technik - Allgemein- und Gesamtdarstellungen (PPN619875100)de
dc.subject.gokfullBiochemie / Physiologische Chemie / Pathobiochemie - Allgemein- und Gesamtdarstellungen (PPN619875313)de
dc.description.embargoed2013-09-13de
dc.identifier.ppn766821927


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