A Study of the chaperonin TCP-1 in mammalian cells: Investigating GFP-tagged CCTε monomer interactions with the Cytoskeleton

Examensarbete för masterexamen

Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12380/140844
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dc.contributor.authorAbdollahi Lakelayeh, Mona
dc.contributor.departmentChalmers tekniska högskola / Institutionen för kemi- och biotekniksv
dc.contributor.departmentChalmers University of Technology / Department of Chemical and Biological Engineeringen
dc.date.accessioned2019-07-03T12:34:44Z-
dc.date.available2019-07-03T12:34:44Z-
dc.date.issued2011
dc.identifier.urihttps://hdl.handle.net/20.500.12380/140844-
dc.description.abstractThe cytosolic chaperonin containing TCP-1, (CCT) is an essential hexadecameric protein consisting of two back-to-back rings each composed of 8-9 subunits. CCT is essential for correct folding of actin and tubulin in order for them to adopt native conformation. However, the role of CCT in cytoskeletal organization is to be further elucidated. The role of CCTε subunit in binding and folding of both actin and tubulin, while it is within the oligomer has been established. This study aimed to investigate CCT ε interactions -as a free monomer -with F-actin and microtubules. In this study, GFP tag, owing to its intrinsic fluorescent property was used for the purpose of rendering CCT ε incapable of being incorporated into the oligomer, thereby allowing its tracing as a free monomer within the cell. A GFP-tagged CCT ε construct was successfully transfected into murine BALB-3T3 and sucrose gradient fractionation confirmed that it was not incorporated into the CCT oligomer. Immunofluorescence staining of the cells for F-actin and microtubules did not reveal any co-localization of GFP tagged-CCTε to filamentous actin or microtubules. A previous study provided evidence that CCTε co-localizes to F-actin, therefore the absence of co-localization between GFP-tagged CCT ε may be due to the conformational alterations arising from GFP fusion to CCTε. The levels of CCT subunits α, β, γ, ε, η were compared between control cells and cells transfected with GFP-tagged CCTε using Image J analysis program in a single attempt. CCT β, γ, and η showed reduced levels in transfected cells. A previous study demonstrated that CCT is up-regulated during growth, therefore the lower levels of subunits in transfected cells may be due to the different cell cycle stages the cells were undergoing, with the control cells probably being in the growth phase.
dc.language.isoeng
dc.setspec.uppsokPhysicsChemistryMaths
dc.subjectLivsvetenskaper
dc.subjectIndustriell bioteknik
dc.subjectLife Science
dc.subjectIndustrial Biotechnology
dc.titleA Study of the chaperonin TCP-1 in mammalian cells: Investigating GFP-tagged CCTε monomer interactions with the Cytoskeleton
dc.type.degreeExamensarbete för masterexamensv
dc.type.degreeMaster Thesisen
dc.type.uppsokH
Collection:Examensarbeten för masterexamen // Master Theses



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