{"id":{"repo_id":"uthsc","oai_identifier":"oai:digitalcommons.library.tmc.edu:utgsbs_dissertations-2519"},"canonical_url":"https://search.dev.ndltd.org/etd/uthsc/oai:digitalcommons.library.tmc.edu:utgsbs_dissertations-2519","repository":{"repo_id":"uthsc","name":"University of Texas Health Science Center at Houston","base_url":"https://digitalcommons.library.tmc.edu/do/oai/"},"display":{"title":"Use of the Protein Misfolding Cyclic Amplification for food safety and drug discovery","abstract":"<p>Prion diseases are fatal neurodegenerative disorders caused by the misfolding of the normal prion protein (PrP<sup>C</sup>) into its infectious form (PrP<sup>Sc</sup>). While the zoonotic potential of chronic wasting disease (CWD) remains uncertain, the presence of prions in food products raises public health concerns. Additionally, therapeutic strategies for prion diseases remain limited. This thesis presents a methodological exploration of the Protein Misfolding Cyclic Amplification (PMCA) technique to address these challenges in two key areas: (1) detecting CWD prions in processed meats subjected to common cooking procedures, and (2) identifying potential anti-prion compounds through a high-throughput PMCA adaptation.</p> <p>Our results demonstrate that PMCA effectively detected CWD prions in a range of processed meat products, with an unexpected increase in prion detectability following grilling and boiling, suggesting enhanced prion accessibility post-cooking. Despite this, these prions failed to convert the human prion protein in PMCA reactions, indicating a limited zoonotic risk under the conditions/materials tested.</p> <p>In parallel, a modified 96-well plate PMCA screening strategy identified eight promising compounds with inhibitory effects on PrP<sup>Sc </sup>formation. Notably, these candidates exhibited diverse properties, including both hydrophilic and hydrophobic profiles, with some compounds previously linked to amyloidogenic pathway inhibition.</p> <p>This study highlights the versatility of the PMCA technique for both, food safety assessments and screening anti-prion compounds. The results presented in this thesis work stress the importance of exploring prion strain diversity, refining PMCA protocols, and validating potential inhibitors in <em>in vivo</em> models for future therapeutic development.</p>","abstract_html":"&lt;p&gt;Prion diseases are fatal neurodegenerative disorders caused by the misfolding of the normal prion protein (PrP&lt;sup&gt;C&lt;/sup&gt;) into its infectious form (PrP&lt;sup&gt;Sc&lt;/sup&gt;). While the zoonotic potential of chronic wasting disease (CWD) remains uncertain, the presence of prions in food products raises public health concerns. Additionally, therapeutic strategies for prion diseases remain limited. This thesis presents a methodological exploration of the Protein Misfolding Cyclic Amplification (PMCA) technique to address these challenges in two key areas: (1) detecting CWD prions in processed meats subjected to common cooking procedures, and (2) identifying potential anti-prion compounds through a high-throughput PMCA adaptation.&lt;/p&gt; &lt;p&gt;Our results demonstrate that PMCA effectively detected CWD prions in a range of processed meat products, with an unexpected increase in prion detectability following grilling and boiling, suggesting enhanced prion accessibility post-cooking. Despite this, these prions failed to convert the human prion protein in PMCA reactions, indicating a limited zoonotic risk under the conditions/materials tested.&lt;/p&gt; &lt;p&gt;In parallel, a modified 96-well plate PMCA screening strategy identified eight promising compounds with inhibitory effects on PrP&lt;sup&gt;Sc &lt;/sup&gt;formation. Notably, these candidates exhibited diverse properties, including both hydrophilic and hydrophobic profiles, with some compounds previously linked to amyloidogenic pathway inhibition.&lt;/p&gt; &lt;p&gt;This study highlights the versatility of the PMCA technique for both, food safety assessments and screening anti-prion compounds. The results presented in this thesis work stress the importance of exploring prion strain diversity, refining PMCA protocols, and validating potential inhibitors in &lt;em&gt;in vivo&lt;/em&gt; models for future therapeutic development.&lt;/p&gt;","abstract_has_math":false,"creators":["Benavente Garcia-Huidobro, Maria R","<p>0009-0000-0271-9674</p>"],"institution":null,"degree_name":"Masters of Science (MS)","degree_level":"Thesis (MS)","degree_discipline":null,"degree_department":null,"school":null,"contributors":["Rodrigo Morales","Seung-Hee Yoo","Kartik Venkatachalam"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2025,"date_issued":"2025-08-01T07:00:00Z","date_published":"2025-08-01T07:00:00Z","updated_at":"2026-07-24T05:49:08Z","subjects":["Prion","drug discovery","food safety","Protein misfolding cyclic amplification","Chronic wasting disease","zoonosis","Animal Sciences","Biology","Food Science","Molecular Biology"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://digitalcommons.library.tmc.edu/utgsbs_dissertations/1462","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Rodrigo Morales","Seung-Hee Yoo","Kartik Venkatachalam"]},{"key":"dc:creator","label":"Author","values":["Benavente Garcia-Huidobro, Maria R","<p>0009-0000-0271-9674</p>"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.available","label":"Dc Date Available","values":["2025-05-22T07:00:00Z"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Thesis (MS)"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Masters of Science (MS)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Prion","drug discovery","food safety","Protein misfolding cyclic amplification","Chronic wasting disease","zoonosis","Animal Sciences","Biology","Food Science","Molecular Biology"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://digitalcommons.library.tmc.edu/utgsbs_dissertations/1462"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["<p>Prion diseases are fatal neurodegenerative disorders caused by the misfolding of the normal prion protein (PrP<sup>C</sup>) into its infectious form (PrP<sup>Sc</sup>). While the zoonotic potential of chronic wasting disease (CWD) remains uncertain, the presence of prions in food products raises public health concerns. Additionally, therapeutic strategies for prion diseases remain limited. This thesis presents a methodological exploration of the Protein Misfolding Cyclic Amplification (PMCA) technique to address these challenges in two key areas: (1) detecting CWD prions in processed meats subjected to common cooking procedures, and (2) identifying potential anti-prion compounds through a high-throughput PMCA adaptation.</p> <p>Our results demonstrate that PMCA effectively detected CWD prions in a range of processed meat products, with an unexpected increase in prion detectability following grilling and boiling, suggesting enhanced prion accessibility post-cooking. Despite this, these prions failed to convert the human prion protein in PMCA reactions, indicating a limited zoonotic risk under the conditions/materials tested.</p> <p>In parallel, a modified 96-well plate PMCA screening strategy identified eight promising compounds with inhibitory effects on PrP<sup>Sc </sup>formation. Notably, these candidates exhibited diverse properties, including both hydrophilic and hydrophobic profiles, with some compounds previously linked to amyloidogenic pathway inhibition.</p> <p>This study highlights the versatility of the PMCA technique for both, food safety assessments and screening anti-prion compounds. The results presented in this thesis work stress the importance of exploring prion strain diversity, refining PMCA protocols, and validating potential inhibitors in <em>in vivo</em> models for future therapeutic development.</p>"]},{"key":"dc:title","label":"Title","values":["Use of the Protein Misfolding Cyclic Amplification for food safety and drug discovery"]}]}],"canonical_facts":{"dc:contributor":["Rodrigo Morales","Seung-Hee Yoo","Kartik Venkatachalam"],"dc:creator":["Benavente Garcia-Huidobro, Maria R","<p>0009-0000-0271-9674</p>"],"dc:date.available":["2025-05-22T07:00:00Z"],"dc:description.abstract":["<p>Prion diseases are fatal neurodegenerative disorders caused by the misfolding of the normal prion protein (PrP<sup>C</sup>) into its infectious form (PrP<sup>Sc</sup>). While the zoonotic potential of chronic wasting disease (CWD) remains uncertain, the presence of prions in food products raises public health concerns. Additionally, therapeutic strategies for prion diseases remain limited. This thesis presents a methodological exploration of the Protein Misfolding Cyclic Amplification (PMCA) technique to address these challenges in two key areas: (1) detecting CWD prions in processed meats subjected to common cooking procedures, and (2) identifying potential anti-prion compounds through a high-throughput PMCA adaptation.</p> <p>Our results demonstrate that PMCA effectively detected CWD prions in a range of processed meat products, with an unexpected increase in prion detectability following grilling and boiling, suggesting enhanced prion accessibility post-cooking. Despite this, these prions failed to convert the human prion protein in PMCA reactions, indicating a limited zoonotic risk under the conditions/materials tested.</p> <p>In parallel, a modified 96-well plate PMCA screening strategy identified eight promising compounds with inhibitory effects on PrP<sup>Sc </sup>formation. Notably, these candidates exhibited diverse properties, including both hydrophilic and hydrophobic profiles, with some compounds previously linked to amyloidogenic pathway inhibition.</p> <p>This study highlights the versatility of the PMCA technique for both, food safety assessments and screening anti-prion compounds. The results presented in this thesis work stress the importance of exploring prion strain diversity, refining PMCA protocols, and validating potential inhibitors in <em>in vivo</em> models for future therapeutic development.</p>"],"dc:identifier":["https://digitalcommons.library.tmc.edu/utgsbs_dissertations/1462"],"dc:subject":["Prion","drug discovery","food safety","Protein misfolding cyclic amplification","Chronic wasting disease","zoonosis","Animal Sciences","Biology","Food Science","Molecular Biology"],"dc:title":["Use of the Protein Misfolding Cyclic Amplification for food safety and drug discovery"],"thesis:degree_level":["Thesis (MS)"],"thesis:degree_name":["Masters of Science (MS)"]},"updated_at":"2026-07-24T05:49:08Z"}