{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/31924"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/31924","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Single molecule pull-down of viral RNA-protein complexes","abstract":"Protein and RNA molecules interact with multiple protein partners to perform essential cellular processes such as post-transcriptional regulation of mRNA. Recently, a single molecule pull-down (SiMPull) assay was developed to isolate and study single protein complexes directly from cell lysates. Unlike ensemble measurements, SiMPull is a powerful tool that allows detection of diverse proteins present in a single complex and quantitation of the number of interacting partners when the proteins are stoichiometrically labeled. Using a similar principle, the objective of this study is to extend the SiMPull assay to isolate and study single cellular RNA-protein complexes. Utilizing a biological system of virally infected mammalian cells, the substrate targeted in the study are viral RNA-protein complexes. Specifically, the highly replicative sendai virus sub-genomic defective interfering (DI) RNA is targeted. The viral DI RNA associates with multiple viral proteins during replication, and is therefore expected to form heterogeneous RNA-protein complexes. Using the RNA sequence information of DI RNA, we designed several short complementary DNA probes to capture single DI RNA molecules for detection with single molecule fluorescence microscopy. We demonstrate specific capture of viral DI RNA molecules using SiMPull, and could quantitatively measure the presence of interacting viral proteins. Therefore, this study provides evidence for the applicability of SiMPull to isolate and study single cellular RNA-protein interactions.","abstract_html":"Protein and RNA molecules interact with multiple protein partners to perform essential cellular processes such as post-transcriptional regulation of mRNA. Recently, a single molecule pull-down (SiMPull) assay was developed to isolate and study single protein complexes directly from cell lysates. Unlike ensemble measurements, SiMPull is a powerful tool that allows detection of diverse proteins present in a single complex and quantitation of the number of interacting partners when the proteins are stoichiometrically labeled. Using a similar principle, the objective of this study is to extend the SiMPull assay to isolate and study single cellular RNA-protein complexes. Utilizing a biological system of virally infected mammalian cells, the substrate targeted in the study are viral RNA-protein complexes. Specifically, the highly replicative sendai virus sub-genomic defective interfering (DI) RNA is targeted. The viral DI RNA associates with multiple viral proteins during replication, and is therefore expected to form heterogeneous RNA-protein complexes. Using the RNA sequence information of DI RNA, we designed several short complementary DNA probes to capture single DI RNA molecules for detection with single molecule fluorescence microscopy. We demonstrate specific capture of viral DI RNA molecules using SiMPull, and could quantitatively measure the presence of interacting viral proteins. Therefore, this study provides evidence for the applicability of SiMPull to isolate and study single cellular RNA-protein interactions.","abstract_has_math":false,"creators":["Srinivasan, Divya"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"M.S.","degree_level":"Thesis","degree_discipline":"Biochemistry","degree_department":null,"school":null,"contributors":["Ha, Taekjip"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2012,"date_issued":"2012-06-27T21:19:38Z","date_published":"2012-06-27T21:19:38Z","updated_at":"2026-07-22T22:25:30Z","subjects":["single molecule","viral RNA","total internal reflection fluorescence microscopy","Ribonucleic acid (RNA)"],"languages":["en"],"rights":["Copyright 2012 Divya Srinivasan"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/2142/31924","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Ha, Taekjip"]},{"key":"dc:creator","label":"Author","values":["Srinivasan, Divya"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2012-06-27T21:19:38Z","2014-06-28T10:00:19Z","2012-05"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Biochemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Thesis"]},{"key":"thesis:degree_name","label":"Degree Name","values":["M.S."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["single molecule","viral RNA","total internal reflection fluorescence microscopy","Ribonucleic acid (RNA)"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright 2012 Divya Srinivasan"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/31924"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Protein and RNA molecules interact with multiple protein partners to perform essential cellular processes such as post-transcriptional regulation of mRNA. 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Using the RNA sequence information of DI RNA, we designed several short complementary DNA probes to capture single DI RNA molecules for detection with single molecule fluorescence microscopy. We demonstrate specific capture of viral DI RNA molecules using SiMPull, and could quantitatively measure the presence of interacting viral proteins. Therefore, this study provides evidence for the applicability of SiMPull to isolate and study single cellular RNA-protein interactions.","Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2012-04-24T14:29:38Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: 1 Srinivasan_Divya.pdf: 5926559 bytes, checksum: 417da5620b02262acfbc1e917cab2817 (MD5)","Made available in DSpace on 2012-06-27T21:19:38Z (GMT). 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