Show simple item record

dc.contributor.advisorMoore, D. Blaine, 1972-
dc.contributor.authorJanuszewski, Jacob
dc.date.accessioned2009-04-10T19:09:42Z
dc.date.available2009-04-10T19:09:42Z
dc.date.issued2005
dc.identifier.urihttp://hdl.handle.net/10920/8045
dc.description.abstractAlzheimer's disease (AD) is its most common form of dementia affecting the elderly population. It is speculated that one of the essential upstream mediators of AD is the accumulation of amyloid beta (Aβ)-containing plaques in the brain. Ab is derived from the cleavage of the amyloid precursor protein (APP) by β-and γ-secretases. On the contrary, there exists a competing pathway to that of the β-and y-secretases, in which another enzyme called α-secretase cleaves APP within the Aβ region. The result of this cleavage precludes plaque formation in the brain, and produces a non-pathogenic sAPPα fragment. TACE (TNF-α Converting Enzyme) is a well known a-secretase that competes with the AD-causing β-and γ-secretase pathway. Thus, elucidating the mechanism of TACE regulation will potentially play an important role in understanding ways to reduce the amount of Ab produced in disease states. Recent in vitro studies have shown that protein kinase C (PKC) is directly involved in the phosphorylation of the TACE cytoplasmic domain. In order to determine if the cytoplasmic domain of TACE plays a significant role in in vivo PKC-mediated phosphorylation, several mutant versions of the TACE cytoplasmic domain were produced for transfection into TACE knockout fibroblasts. Since this lab has not yet shown if the TACE knockout fibroblasts are transfectable, this became an important factor in the experiment. Here we show that TACE knockout fibroblasts are transfectable, and that cellular detection of equivalent levels of epitope-tagged TACE constructs is possible. Experiments are ongoing to determine if our mutant TACE constructs will produce altered levels of sAPPα. Wild type or mutant TACE constructs will be expressed and then stimulated with PMA to determine if the mutant version of TACE reduces the amount of sAPPα produced.
dc.description.sponsorshipKalamazoo Collegeen
dc.description.sponsorshipDepartment of Biology, Kalamazoo College
dc.description.sponsorshipKalamazoo College. Department of Biology. Diebold Symposium, 2005
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen
dc.publisherKalamazoo, Mich. : Kalamazoo College.en
dc.relation.ispartofKalamazoo College Diebold Symposium Presentations Collection
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.
dc.titleExpression of Mutant Epitope-Tagged TACE Constructs in TACE Knockout Fibroblasts and the Importance of TACE Cytoplasmic Domain in PKC-Mediated Phosphorylationen
dc.typePresentationen


Files in this item

Thumbnail

This item appears in the following Collection(s)

  • Diebold Symposium Posters and Schedules [320]
    Poster and oral presentations by senior biology majors that include the results of their Senior Individualized Projects (SIPs) at the Diebold Symposium. Abstracts are generally available to the public, but PDF files are available only to current Kalamazoo College students, faculty, and staff.

Show simple item record