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dc.contributor.authorKukday, Sayali Shrikant
dc.date.accessioned2014-03-04T20:36:15Z
dc.date.available2014-03-04T20:36:15Z
dc.date.issued2012-08
dc.identifier.otherkukday_sayali_s_201208_phd
dc.identifier.urihttp://purl.galileo.usg.edu/uga_etd/kukday_sayali_s_201208_phd
dc.identifier.urihttp://hdl.handle.net/10724/28313
dc.description.abstractThe insulin-degrading enzyme (IDE), a Zn2+-dependent metalloprotease, degrades several physiologically important peptides including Aβ, a peptide involved in the pathogenesis of Alzheimer’s disease. Enhancing IDE activity may be therapeutically beneficial because it would lead to increased clearance of Aβ thereby minimizing its toxic effects. In this study, small-molecule activators of IDE were identified by means of a high-throughput screen, using rat IDE and a synthetic fluorogenic reporter. The results demonstrate that IDE activators exhibit substrate and species specificity, which was observed upon comparing the effects of activators on various IDE orthologs and in the context of distinct reporters. The results of a high-throughput screen aimed at identifying small-molecule activators of human IDE using a novel Aβ synthetic fluorogenic reporter are also discussed. This study provides insight into the various considerations that should be taken into account during the design of high-throughput screens aimed at identifying IDE activators. This study also indicates that activators can be substrate-specific thereby minimizing the impact on other IDE substrates including insulin.
dc.languageeng
dc.publisheruga
dc.rightspublic
dc.subjectAlzheimer’s disease
dc.subject
dc.subjectinsulin-degrading enzyme
dc.subjectactivator
dc.subjectprotease
dc.subjecthigh-throughput screen
dc.subjectfluorescence
dc.subjectyeast
dc.subjecta-factor
dc.titleModulating insulin-degrading enzyme activity
dc.title.alternativeimplications for identifying activators through high-throughput screening
dc.typeDissertation
dc.description.degreePhD
dc.description.departmentBiochemistry and Molecular Biology
dc.description.majorBiochemistry and Molecular Biology
dc.description.advisorWalter Schmidt
dc.description.committeeWalter Schmidt
dc.description.committeeLance Wells
dc.description.committeeClaiborne Glover
dc.description.committeeMarcus Fechheimer


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