Timekeeper: Advancing Circadian Research with GST-Tagged Per3 Protein

dc.contributor.advisorArribas, Raquel
dc.contributor.authorAlanezi, Sarah Abdullah
dc.date.accessioned2024-12-04T07:03:57Z
dc.date.issued2024
dc.description.abstractThe Per3 gene plays a crucial role in regulating circadian rhythms, profoundly impacting sleep-wake cycles and metabolic processes. Despite its biological significance, the expression and purification of Per3 have presented substantial challenges, often resulting in low yields and poor solubility. This study tackles these obstacles by employing innovative cloning and expression techniques, particularly utilizing a GST-Per3long to enhance solubility and purification efficiency. We designed primers incorporating homology regions complementary to restriction enzyme-digested ends and employed the In-Fusion cloning method to integrate the Per3 gene into the p3E plasmid vector with high precision. The transformation efficiencies were remarkable, with colony counts reaching 2.292 x 10^8 colonies per μg of plasmid DNA. PCR amplification confirmed the successful integration of the Per3 gene, with distinct bands observed at the expected size of 1143 bp, which was further confirmed by DNA sequencing. Protein expression trials identified 25°C as the optimal temperature, significantly improving the yield and solubility of the GST-tagged Per3 protein. Subsequent purification through GST Affinity chromatography and gel filtration chromatography yielded a highly pure protein, as confirmed by SDS-PAGE and native gel electrophoresis. Although the initial yield was modest, the high purity of the purified protein provides a robust foundation for future functional and structural studies. This study not only establishes a reliable protocol for Per3 expression and purification but also opens avenues for investigating the interactions of Per3 with other circadian proteins, such as CRY and BMAL1, to determine their mutual exclusivity and relative affinity. These interactions are crucial for understanding the biological role of Per3 in fine-tuning the circadian clock. Future work should focus on optimizing expression conditions to further increase yield and investigate the intricate biological activity of the Per3 protein within the circadian network.
dc.format.extent55
dc.identifier.citationAPA
dc.identifier.urihttps://hdl.handle.net/20.500.14154/74014
dc.language.isoen
dc.publisherThe University of Edinburgh
dc.subjectCircadian Rhythm
dc.subjectBiological Clock
dc.subjectSleep-Wake Cycle
dc.subjectPer3 Protein
dc.subjectCircadian Clock Proteins
dc.subjectMolecular Cloning
dc.subjectRecombinant Protein Expression
dc.subjectGST-Tag Fusion Protein
dc.subjectEscherichia coli
dc.subjectIn-Fusion Cloning
dc.subjectProtein Solubility
dc.subjectGene Expression
dc.subjectChronotherapy
dc.subjectProtein-Protein Interactions
dc.subjectCellular Timekeeping
dc.subjectChronobiology
dc.subjectMolecular Biology
dc.subjectBiochemistry
dc.subjectGene Regulation
dc.subjectGenetic Engineering
dc.subjectProtein Purification
dc.subjectPCR Validation
dc.subjectCloning Techniques
dc.subjectSoluble Protein Production
dc.subjectCircadian Biology
dc.subjectCellular Rhythms
dc.subjectMolecular Timekeeping
dc.subjectBiological Rhythms
dc.subjectTranscriptional Feedback Loops
dc.subjectClock Gene Interactions
dc.subjectProtein Complexes
dc.subjectGene-Protein Networks
dc.subjectCircadian Disorders
dc.subjectMetabolic Regulation
dc.subjectSleep Disorders
dc.subjectRhythmic Gene Expression
dc.subjectChronomedicine
dc.subjectCellular Oscillators
dc.subjectClock Protein Mechanisms
dc.subjectFunctional Genomics
dc.titleTimekeeper: Advancing Circadian Research with GST-Tagged Per3 Protein
dc.typeThesis
sdl.degree.departmentBiological Sciences
sdl.degree.disciplineBiochemistry
sdl.degree.grantorThe University of Edinburgh
sdl.degree.nameMaster of Science

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