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Development of Activity-based Reporter Gene Technology (AbRGT) for Imaging of Protease Activity and its Applications

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dc.contributor.advisor BRITTO, SANDANARAJ S. en_US
dc.contributor.author BATHLA, PUNITA en_US
dc.date.accessioned 2021-05-28T08:44:59Z
dc.date.available 2021-05-28T08:44:59Z
dc.date.issued 2021-05 en_US
dc.identifier.citation 154 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5906
dc.description.abstract Fluorescence 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.sponsorship IISER Pune Department of Biotechnology (DBT) Infosys travel award en_US
dc.language.iso en en_US
dc.subject AbRGT en_US
dc.subject FRET en_US
dc.subject BRET en_US
dc.subject Caspase en_US
dc.subject Caspase-3 en_US
dc.subject High-throughput screening en_US
dc.subject Protease activity en_US
dc.subject Activity based probes en_US
dc.subject Fluorescence en_US
dc.subject Bioluminescence en_US
dc.subject Apoptosis pathway en_US
dc.subject Inhibitors screening en_US
dc.title Development of Activity-based Reporter Gene Technology (AbRGT) for Imaging of Protease Activity and its Applications en_US
dc.type Thesis en_US
dc.publisher.department Dept. of Biology en_US
dc.type.degree Int.Ph.D en_US
dc.contributor.department Dept. of Biology en_US
dc.contributor.registration 20142003 en_US


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  • PhD THESES [603]
    Thesis submitted to IISER Pune in partial fulfilment of the requirements for the degree of Doctor of Philosophy

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