Yüksek Lisans Tezleri
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/5799
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Master Thesis Escherichia Coli Konak Organizmada GLP-1 Analoğunun Rekombinant Üretimi(Abdullah Gül Üniversitesi, Fen Bilimleri Enstitüsü, 2024) Çalış, Burak; Fidan, ÖzkanDiabetes is the most serious metabolic disorder correlated with obesity, hypertension and cardiovascular conditions. High prevalence of Type II Diabetes Mellitus (T2DM) indicates the need for new medication development. In developing therapeutics, higher efficiency and fewer adverse effect features are targeted primarily. Recombinant protein-based biotechnological drug molecules have been developed and used for the treatment of T2DM. Especially, GLP-1 analogues are known by their self-limiting mechanism and insulinotropic effect. In this study, a novel GLP-1 analogue with increased stability and efficiency is produced using recombinant E. coli. The expression plasmid was constructed and confirmed by restriction digestion and whole plasmid sequencing. Then, itwas transformed into various E. coli strains followed by optimized lysis, growth and expression conditions to maximize the yield of the GLP-1 analogue. Various parameters such as pre-induction time, induction point, induction IPTG concentration and post-induction temperature were tested for the succesfull expression with maximum yield. Consequently, it was achieved that E. coli BL21(DE3) as strain, 0.2 mM IPTG induction at OD600nm of 0.6 and 18 °C overnight post-induction growth was the most promising conditions. Under these conditions, the GLP-1 analogue was obtained in the insoluble fraction. Following protein analysis and purification, quantification was performed and the highest titer of GLP-1 analogue was measured as 626 µg/ml. As future prospect, using another host organism and changing growth conditions can provide obtaining target protein in the soluble form. Keywords: T2DM, GLP-1 analogue, recombinant DNA technology, protein expression, E. coliMaster Thesis Potansiyel Gen Dağıtımı Uygulamaları için Poegma ve Sistaminle Modifiye Plazmit DNA'lar İçeren Polimerik Konjugatlar(Abdullah Gül Üniversitesi, Fen Bilimleri Enstitüsü, 2024) Yıldız, Gizem; İşoğlu, İsmail Alper; İşoğlu, Sevil DinçerPolymer-based gene delivery systems have revealed significant advancements in the treatment of various diseases in recent years. Considering the potential of polymeric vectors, it is observed that the improvements in the field of gene therapy enable effective gene transfection and induced therapeutic protein production. In this thesis study, a strategy based on a new conjugation procedure is designed to increase the gene transfer and cellular uptake rate of plasmid DNAs. According to the findings, POEGMA-based carrier and cystamine-modified plasmid DNAs demonstrated successful conjugation through disulfide bond formation. MDA-MB-231 in vitro cellular uptake results of conjugates showed 94-98% cell internalization, indicating excellent results compared to the well-known polymers in the literature. As a result, the new delivery system we developed in this study determined the success of cystamine-modified plasmid DNAs binding to POEGMA polymer chains via a covalent linkage for the first time in the literature and provided a start for future studies.Master Thesis İn Siliko Analizlerle Yeni Patojenik Varyantlar Bulmak(Abdullah Gül Üniversitesi, Fen Bilimleri Enstitüsü, 2022) Zorluer, Ziya Furkan; Kaplan, Oktay İsmailInherited diseases are health problems caused by one or more abnormalities in the genome. It can be caused by changes in a single gene (monogenic) or multiple genes (polygenic), or by a damage on chromosomes. Genetic variation is the differences in the DNA sequences that can be observed within a species or in alleles. Evaluation of genetic variants, together with reported phenotypic or pathogenic annotations from non-human organisms, facilitates the comparison of these variants with their human counterparts. In this work, we combined pathogenic and phenotypic annotations with variants, and these phenotypic orthologous variants from seven organisms can provide clues to the functional consequences of human genetic variants.
