Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5906
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dc.contributor.advisorBRITTO, SANDANARAJ S.en_US
dc.contributor.authorBATHLA, PUNITAen_US
dc.date.accessioned2021-05-28T08:44:59Z-
dc.date.available2021-05-28T08:44:59Z-
dc.date.issued2021-05en_US
dc.identifier.citation154en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5906-
dc.description.abstractFluorescence imaging methods integrated with substrate-based reporter assays (both genetic and synthetic substrate) are routinely used to study the function of “active protease” in the (patho) physiological processes. However, most of the substrate-based reporters lack target specificity in the in vivo conditions. Recently, the activity-based fluorescent probe (ABFP) method is used for monitoring protease function in vivo. This method provides an opportunity to back-track the signal produced by the target enzyme and other proteases. However, this is achieved through post-processing of cell or tissue lysate followed by in-gel fluorescence studies. ABFP method is labor-intensive and cannot be translated to high-throughput imaging studies. To address the drawbacks of existing techniques, herein, we disclose the design and development of a new technology called “Activity-based Reporter Gene Technology” (AbRGT). It uses a reporter protein-tagged protease of interest (PoI) and an activity-based fluorescent probe (ABFP). The specific activation of PoI is determined by measuring the fluorescence resonance energy transfer (FRET) signal that occurs only upon labeling of ABFP to the reporter protein-tagged PoI. In this manner, the method allows the imaging of an active protease with an exquisite specificity in the presence of highly homogenous proteins within a cell. As a proof-of concept, we have applied this method to study the function of individual caspase protease in both intrinsic and extrinsic apoptosis signaling pathways. We demonstrate that the same method can be used for profiling of compounds that can inhibit caspases activity. We have also shown the design and potential use of the BRET approach of AbRGT in the high throughput screening of protease inhibitors. Altogether, this method holds huge potential for applications in the area of diagnostics, screening of drugs, and other discovery efforts.en_US
dc.description.sponsorshipIISER Pune Department of Biotechnology (DBT) Infosys travel awarden_US
dc.language.isoenen_US
dc.subjectAbRGTen_US
dc.subjectFRETen_US
dc.subjectBRETen_US
dc.subjectCaspaseen_US
dc.subjectCaspase-3en_US
dc.subjectHigh-throughput screeningen_US
dc.subjectProtease activityen_US
dc.subjectActivity based probesen_US
dc.subjectFluorescenceen_US
dc.subjectBioluminescenceen_US
dc.subjectApoptosis pathwayen_US
dc.subjectInhibitors screeningen_US
dc.titleDevelopment of Activity-based Reporter Gene Technology (AbRGT) for Imaging of Protease Activity and its Applicationsen_US
dc.typeThesisen_US
dc.publisher.departmentDept. of Biologyen_US
dc.type.degreeInt.Ph.Den_US
dc.contributor.departmentDept. of Biologyen_US
dc.contributor.registration20142003en_US
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