{"id":{"repo_id":"kennesaw","oai_identifier":"oai:digitalcommons.kennesaw.edu:mscs_etd-1052"},"canonical_url":"https://search.dev.ndltd.org/etd/kennesaw/oai:digitalcommons.kennesaw.edu:mscs_etd-1052","repository":{"repo_id":"kennesaw","name":"Kennesaw State University","base_url":"https://digitalcommons.kennesaw.edu/do/oai/"},"display":{"title":"Analyzing the interactions of thermoresponsive coacervate-forming biodegradable polyester encapsulation on model protein structure and activity","abstract":"<p>Protein therapeutics hold high efficacy in treatment for various diseases including cancer and diabetes. However, the treatment cost is generally higher than other therapeutics mainly due to <em>in vivo</em> protein degradation. This drawback creates demand for more efficient delivery methods to preserve the function and integrity of protein therapeutics. Thermoresponsive coacervate-forming biodegradable polyesters (TR-PEs) are a thermoresponsive molecular packaging system used in protein therapeutic research. The term coacervate refers to a phase-separated solution in which a dense polymer phase separates from the aqueous phase to form nanodroplets within solution, capturing bioactive molecules. Limited research demonstrates if TR-PEs can encapsulate and preserve a larger protein’s activity and how these TR-PEs interact with a protein on the biophysical level. It was determined that TR-PEs encapsulated and released active β-galactosidase enzyme. Encapsulation was visualized using confocal fluorescence microscopy and by labeling β-galactosidase with fluorescein isothiocyanate. Interactions between <sup>15</sup>N-isotopically labelled human ubiquitin c and TR-PEs were investigated through variable temperature nuclear magnetic resonance. It was interpreted that TR-PEs non-specifically interact with <sup>15</sup>N-ubiquitin and that various pendant groups within a given polymer resulted in non-significant differences. Although TR-PEs may not be specifically interacting with the model cargos, demonstrating that TR-PEs capture and release an unaltered, complex protein exemplifies the viability of using TR-PEs for future therapeutic packaging and possible delivery.</p>","abstract_html":"&lt;p&gt;Protein therapeutics hold high efficacy in treatment for various diseases including cancer and diabetes. However, the treatment cost is generally higher than other therapeutics mainly due to &lt;em&gt;in vivo&lt;/em&gt; protein degradation. This drawback creates demand for more efficient delivery methods to preserve the function and integrity of protein therapeutics. Thermoresponsive coacervate-forming biodegradable polyesters (TR-PEs) are a thermoresponsive molecular packaging system used in protein therapeutic research. The term coacervate refers to a phase-separated solution in which a dense polymer phase separates from the aqueous phase to form nanodroplets within solution, capturing bioactive molecules. Limited research demonstrates if TR-PEs can encapsulate and preserve a larger protein’s activity and how these TR-PEs interact with a protein on the biophysical level. It was determined that TR-PEs encapsulated and released active β-galactosidase enzyme. Encapsulation was visualized using confocal fluorescence microscopy and by labeling β-galactosidase with fluorescein isothiocyanate. Interactions between &lt;sup&gt;15&lt;/sup&gt;N-isotopically labelled human ubiquitin c and TR-PEs were investigated through variable temperature nuclear magnetic resonance. It was interpreted that TR-PEs non-specifically interact with &lt;sup&gt;15&lt;/sup&gt;N-ubiquitin and that various pendant groups within a given polymer resulted in non-significant differences. Although TR-PEs may not be specifically interacting with the model cargos, demonstrating that TR-PEs capture and release an unaltered, complex protein exemplifies the viability of using TR-PEs for future therapeutic packaging and possible delivery.&lt;/p&gt;","abstract_has_math":false,"creators":["Casterline, Conner"],"institution":null,"degree_name":"Master of Science in Chemical Sciences (MSCB)","degree_level":"Thesis","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":["Thomas C. Leeper","Carol A. Chrestensen","Christopher R. Dockery"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2022,"date_issued":"2022-05-12T07:00:00Z","date_published":"2022-05-12T07:00:00Z","updated_at":"2026-07-24T02:43:58Z","subjects":["Therapeutic encapsulation","enzymatic activity","confocal microscopy","Chemistry"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://digitalcommons.kennesaw.edu/mscs_etd/51","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Thomas C. Leeper","Carol A. Chrestensen","Christopher R. 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However, the treatment cost is generally higher than other therapeutics mainly due to <em>in vivo</em> protein degradation. This drawback creates demand for more efficient delivery methods to preserve the function and integrity of protein therapeutics. Thermoresponsive coacervate-forming biodegradable polyesters (TR-PEs) are a thermoresponsive molecular packaging system used in protein therapeutic research. The term coacervate refers to a phase-separated solution in which a dense polymer phase separates from the aqueous phase to form nanodroplets within solution, capturing bioactive molecules. Limited research demonstrates if TR-PEs can encapsulate and preserve a larger protein’s activity and how these TR-PEs interact with a protein on the biophysical level. It was determined that TR-PEs encapsulated and released active β-galactosidase enzyme. Encapsulation was visualized using confocal fluorescence microscopy and by labeling β-galactosidase with fluorescein isothiocyanate. Interactions between <sup>15</sup>N-isotopically labelled human ubiquitin c and TR-PEs were investigated through variable temperature nuclear magnetic resonance. It was interpreted that TR-PEs non-specifically interact with <sup>15</sup>N-ubiquitin and that various pendant groups within a given polymer resulted in non-significant differences. Although TR-PEs may not be specifically interacting with the model cargos, demonstrating that TR-PEs capture and release an unaltered, complex protein exemplifies the viability of using TR-PEs for future therapeutic packaging and possible delivery.</p>"]},{"key":"dc:title","label":"Title","values":["Analyzing the interactions of thermoresponsive coacervate-forming biodegradable polyester encapsulation on model protein structure and activity"]}]}],"canonical_facts":{"dc:contributor":["Thomas C. Leeper","Carol A. Chrestensen","Christopher R. Dockery"],"dc:creator":["Casterline, Conner"],"dc:date.available":["2024-05-10T07:00:00Z"],"dc:description.abstract":["<p>Protein therapeutics hold high efficacy in treatment for various diseases including cancer and diabetes. However, the treatment cost is generally higher than other therapeutics mainly due to <em>in vivo</em> protein degradation. This drawback creates demand for more efficient delivery methods to preserve the function and integrity of protein therapeutics. Thermoresponsive coacervate-forming biodegradable polyesters (TR-PEs) are a thermoresponsive molecular packaging system used in protein therapeutic research. The term coacervate refers to a phase-separated solution in which a dense polymer phase separates from the aqueous phase to form nanodroplets within solution, capturing bioactive molecules. Limited research demonstrates if TR-PEs can encapsulate and preserve a larger protein’s activity and how these TR-PEs interact with a protein on the biophysical level. It was determined that TR-PEs encapsulated and released active β-galactosidase enzyme. Encapsulation was visualized using confocal fluorescence microscopy and by labeling β-galactosidase with fluorescein isothiocyanate. Interactions between <sup>15</sup>N-isotopically labelled human ubiquitin c and TR-PEs were investigated through variable temperature nuclear magnetic resonance. It was interpreted that TR-PEs non-specifically interact with <sup>15</sup>N-ubiquitin and that various pendant groups within a given polymer resulted in non-significant differences. Although TR-PEs may not be specifically interacting with the model cargos, demonstrating that TR-PEs capture and release an unaltered, complex protein exemplifies the viability of using TR-PEs for future therapeutic packaging and possible delivery.</p>"],"dc:identifier":["https://digitalcommons.kennesaw.edu/mscs_etd/51"],"dc:subject":["Therapeutic encapsulation","enzymatic activity","confocal microscopy","Chemistry"],"dc:title":["Analyzing the interactions of thermoresponsive coacervate-forming biodegradable polyester encapsulation on model protein structure and activity"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Thesis"],"thesis:degree_name":["Master of Science in Chemical Sciences (MSCB)"]},"updated_at":"2026-07-24T02:43:58Z"}