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Effect of palmitoylated synaptic proteins and biologically relevant calcium concentrations on the compartmentalization of PI(4,5)P2 in membrane model systems and in the plasma membrane of PC12 cells

dc.contributor.advisorFernandes, Fábio
dc.contributor.advisorCoutinho, Ana Isabel Abrantes, 1965-
dc.contributor.authorSarmento, Maria João Martins
dc.date.accessioned2013-07-24T10:08:15Z
dc.date.available2013-07-24T10:08:15Z
dc.date.issued2011
dc.descriptionTese de mestrado em Bioquímica (Bioquímica Médica), apresentada à Universidade de Lisboa, através da Faculdade de Ciências, 2011por
dc.description.abstractPhosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) is a minor component of the plasma membrane of eukaryotic cells that is essential for several cellular mechanisms, including organization of the actin cytoskeleton, membrane trafficking, endocytosis and exocytosis. The regulation of these processes is thought to involve the local enrichment of PI(4,5)P2 in the plasma membrane at particular timings. In the first part of this work, we aimed to better characterize the mechanisms responsible for PI(4,5)P2 clustering in the plasma membrane of neuronal-like (PC12) and non-neuronal (HEK293) cells. Using FRET microscopy carried out with PH-domains labelled with fluorescent proteins (PH-CFP and PG-YFP), we detected a highly clustered distribution of PI(4,5)P2 in PC12 cells and some indication of clustering below the confocal resolution for HEK293 cells. Moreover, FRET efficiency decreased after inhibition of protein palmitoylation, emphasizing the importance of the interaction between palmitoylated proteins and PI(4,5)P2 for its lateral membrane organization. Additionally, since we were also interested in studying PI(4,5)P2 distribution in giant unilamellar vesicles (GUVs), we optimized a GUV immobilization method based on the interaction of biotinylated lipids with an avidin-coated surface. Three different biotinylated lipids were studied: DOPE-Cap-biotin, DPPE-Cap-biotin and DPPE-biotin. Since PI(4,5)P2 has been shown to partition into lipid rafts, studies with POPC:Chol:PSM (1:1:1) GUVs presenting a coexistence of liquid ordered/liquid disordered phases were performed. Our results showed that the immobilization conditions and the type of immobilizing lipid significantly influence the distribution of lipid domains within GUVs, potentially generating artefacts in lipid phase coexistence studies. By imaging GUVs with a fluorescent analogue of PI(4,5)P2, we observed a Ca2+ induced clustering of the fluorescent lipid at concentrations (>100 μM) known to occur in the proximity of calcium channels after synaptic stimulation. Then, PI(4,5)P2 can potentially act as a lipidic calcium sensor, regulating not only local plasma membrane charge and curvature but also synaptic protein organization.por
dc.identifier.urihttp://hdl.handle.net/10451/8859
dc.language.isoengpor
dc.subjectPI(4,5)P2por
dc.subjectDistributionpor
dc.subjectExocytosispor
dc.subjectProtein palmitoylationpor
dc.subjectCalciumpor
dc.subjectGUV immobilizationpor
dc.subjectTeses de mestrado - 2011por
dc.titleEffect of palmitoylated synaptic proteins and biologically relevant calcium concentrations on the compartmentalization of PI(4,5)P2 in membrane model systems and in the plasma membrane of PC12 cellspor
dc.typemaster thesis
dspace.entity.typePublication
rcaap.rightsopenAccesspor
rcaap.typemasterThesispor

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