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A novel tool for neuronal physiology and pathology: optimization of secondary ion mass spectrometry approaches

dc.contributor.advisorRizzoli, Silvio O. Prof. Dr.
dc.contributor.authorAgüí González, Paola
dc.date.accessioned2023-10-05T13:32:22Z
dc.date.available2023-10-08T00:50:11Z
dc.date.issued2023-10-05
dc.identifier.urihttp://resolver.sub.uni-goettingen.de/purl?ediss-11858/14902
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-9903
dc.format.extent110de
dc.language.isoengde
dc.subject.ddc610de
dc.titleA novel tool for neuronal physiology and pathology: optimization of secondary ion mass spectrometry approachesde
dc.typedoctoralThesisde
dc.contributor.refereeRizzoli, Silvio O. Prof. Dr.
dc.date.examination2023-05-11de
dc.description.abstractengSecondary Ion Mass Spectrometry (SIMS) is a powerful tool for characterizing the chemical composition of solid samples and thin films, offering high sensitivity and spatial resolution. While initially developed for geology, cosmochemistry and material science, the continuous evolution of this imaging technique has broadened its scope towards other disciplines, including biology. Despite inherent challenges and limitations in SIMS imaging, through the four projects included in this thesis, I demonstrate that it is possible to perform quantitative biological imaging with this technique, overcoming some of the most important limitations by introducing novel tools and combining SIMS with other imaging techniques. First, Time of Flight Mass Secondary Ion Mass Spectrometry (ToF-SIMS) was employed to investigate the potential correlation between the synaptic activity of hippocampal neurons and the composition and distribution of lipid species on their plasma membranes. Second, I present some novel probes, detectable with both SIMS and fluorescence microscopy, which enabled protein localization at the subcellular level. Third, Nanoscale Secondary Ion Mass Spectrometry (NanoSIMS) was correlated with Transmission Electron Microscopy (TEM), to investigate the inclusion of newly synthesized proteins into mature myelin sheaths. Fourth, we developed and successfully applied a protocol to correlate three imaging techniques. Through a single experiment, this protocol enables the localization of specific targets with light microscopy, the analysis of the morphology of cellular structures with TEM, and the investigation of the chemical composition of regions of interest with NanoSIMS. In summary, the work included in this thesis aims to boost the use of SIMS imaging in neuro- and cell biology, showing how the combination of this technique with new tools and technologies has the potential to enhance our knowledge about cellular mechanisms, as well as facilitating diagnostics and drug development.de
dc.contributor.coRefereeRehling, Peter Prof. Dr.
dc.contributor.thirdRefereeMeyer, Thomas Prof. Dr.
dc.subject.gerSIMSde
dc.subject.gerImage correlationde
dc.subject.gerAnalytical techniquede
dc.subject.gerCell biologyde
dc.subject.engSIMS imagingde
dc.subject.engImage correlationde
dc.subject.engCell biologyde
dc.subject.engAnalytical techniquede
dc.identifier.urnurn:nbn:de:gbv:7-ediss-14902-2
dc.affiliation.instituteMedizinische Fakultätde
dc.subject.gokfullMethoden und Techniken in der Medizin (PPN619875143)de
dc.subject.gokfullNeurologie - Allgemein- und Gesamtdarstellungen (PPN619876247)de
dc.subject.gokfullBiochemie / Physiologische Chemie / Pathobiochemie - Allgemein- und Gesamtdarstellungen (PPN619875313)de
dc.subject.gokfullBiologie (PPN619875151)de
dc.description.embargoed2023-10-08de
dc.identifier.ppn1867413000
dc.identifier.orcid0000-0002-2313-1439de
dc.notes.confirmationsentConfirmation sent 2023-10-05T13:45:01de


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