{"id":{"repo_id":"mit","oai_identifier":"oai:dspace.mit.edu:1721.1/87473"},"canonical_url":"https://search.dev.ndltd.org/etd/mit/oai:dspace.mit.edu:1721.1/87473","repository":{"repo_id":"mit","name":"MIT","base_url":"https://dspace.mit.edu/oai/request"},"display":{"title":"Approaches towards development of novel fluorogenic biosensors for detection of small protein analytes","abstract":"One of the most remarkable ideas in modem biology is that organization of multicellular life is orchestrated by a relatively small repertoire of signaling molecules, which mediate communication between cells. Breakdown of these communication pathways can have profound consequences, leading to a multiplicity of developmental defects and disease states. In particular, the ErbB family of receptors and ligands regulate key cellular processes such as proliferation, differentiation, and apoptosis during embryonic development, cellular homeostasis, and tumorigenesis. The generality of the ErbB-network has made it one of the most well-studied cell signaling systems. However, traditional methods used to study cellular signaling either fail to capture the dynamic nature of signaling networks or to lack the ability to quantify native signaling components. To further our understanding of the signaling processes that govern cell fate and tissue health, novel non-invasive techniques must be developed to quantitatively track native protein analytes in live cells. Herein approaches toward the development of a set novel fluorogenic biosensors capable of detecting native ErbB-ligands are reported. Using yeast surface display, two libraries of protein-binding scaffolds were engineered to bind selectively to human EGF and human betacellulin with low nM KD. Bio-orthogonal conjugation of these protein scaffolds to 4-DMN, a solvatochromic fluorophore, afforded a biosensor that exhibit a 3-fold fluorescence increase upon binding human EGF. Efforts to improve the fluorescent signal via alternative labeling strategies are also reported.","abstract_html":"One of the most remarkable ideas in modem biology is that organization of multicellular life is orchestrated by a relatively small repertoire of signaling molecules, which mediate communication between cells. Breakdown of these communication pathways can have profound consequences, leading to a multiplicity of developmental defects and disease states. In particular, the ErbB family of receptors and ligands regulate key cellular processes such as proliferation, differentiation, and apoptosis during embryonic development, cellular homeostasis, and tumorigenesis. The generality of the ErbB-network has made it one of the most well-studied cell signaling systems. However, traditional methods used to study cellular signaling either fail to capture the dynamic nature of signaling networks or to lack the ability to quantify native signaling components. To further our understanding of the signaling processes that govern cell fate and tissue health, novel non-invasive techniques must be developed to quantitatively track native protein analytes in live cells. Herein approaches toward the development of a set novel fluorogenic biosensors capable of detecting native ErbB-ligands are reported. Using yeast surface display, two libraries of protein-binding scaffolds were engineered to bind selectively to human EGF and human betacellulin with low nM KD. Bio-orthogonal conjugation of these protein scaffolds to 4-DMN, a solvatochromic fluorophore, afforded a biosensor that exhibit a 3-fold fluorescence increase upon binding human EGF. Efforts to improve the fluorescent signal via alternative labeling strategies are also reported.","abstract_has_math":false,"creators":["Cheung, Stephanie, S.M. Massachusetts Institute of Technology"],"institution":"Massachusetts Institute of Technology","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":"Massachusetts Institute of Technology. Department of Chemistry.","school":null,"contributors":[],"advisors":["Barbara Imperiali."],"committee_chairs":[],"committee_members":[],"year":2014,"date_issued":"2014","date_published":"2014","updated_at":"2026-07-22T22:22:16Z","subjects":["Chemistry."],"languages":["eng"],"rights":["M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission."],"rights_urls":["http://dspace.mit.edu/handle/1721.1/7582"],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/1721.1/87473","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Barbara Imperiali."]},{"key":"dc:contributor.department","label":"Department","values":["Massachusetts Institute of Technology. Department of Chemistry."]},{"key":"dc:contributor.other","label":"Dc Contributor Other","values":["Massachusetts Institute of Technology. Department of Chemistry."]},{"key":"dc:creator","label":"Author","values":["Cheung, Stephanie, S.M. Massachusetts Institute of Technology"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2014-05-23T19:35:12Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2014-05-23T19:35:12Z"]},{"key":"dc:date.issued","label":"Date","values":["2014"]},{"key":"dc:publisher","label":"Institution","values":["Massachusetts Institute of Technology"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Chemistry."]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["eng"]},{"key":"dc:rights","label":"Dc Rights","values":["M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission."]},{"key":"dc:rights.uri","label":"Rights URI","values":["http://dspace.mit.edu/handle/1721.1/7582"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/1721.1/87473"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Thesis: S.M., Massachusetts Institute of Technology, Department of Chemistry, 2014.","Cataloged from PDF version of thesis.","Includes bibliographical references."]},{"key":"dc:description.abstract","label":"Abstract","values":["One of the most remarkable ideas in modem biology is that organization of multicellular life is orchestrated by a relatively small repertoire of signaling molecules, which mediate communication between cells. Breakdown of these communication pathways can have profound consequences, leading to a multiplicity of developmental defects and disease states. In particular, the ErbB family of receptors and ligands regulate key cellular processes such as proliferation, differentiation, and apoptosis during embryonic development, cellular homeostasis, and tumorigenesis. The generality of the ErbB-network has made it one of the most well-studied cell signaling systems. However, traditional methods used to study cellular signaling either fail to capture the dynamic nature of signaling networks or to lack the ability to quantify native signaling components. To further our understanding of the signaling processes that govern cell fate and tissue health, novel non-invasive techniques must be developed to quantitatively track native protein analytes in live cells. Herein approaches toward the development of a set novel fluorogenic biosensors capable of detecting native ErbB-ligands are reported. Using yeast surface display, two libraries of protein-binding scaffolds were engineered to bind selectively to human EGF and human betacellulin with low nM KD. Bio-orthogonal conjugation of these protein scaffolds to 4-DMN, a solvatochromic fluorophore, afforded a biosensor that exhibit a 3-fold fluorescence increase upon binding human EGF. Efforts to improve the fluorescent signal via alternative labeling strategies are also reported."]},{"key":"dc:description.degree","label":"Dc Description Degree","values":["S.M."]},{"key":"dc:title","label":"Title","values":["Approaches towards development of novel fluorogenic biosensors for detection of small protein analytes"]}]}],"canonical_facts":{"dc:contributor.advisor":["Barbara Imperiali."],"dc:contributor.department":["Massachusetts Institute of Technology. Department of Chemistry."],"dc:contributor.other":["Massachusetts Institute of Technology. Department of Chemistry."],"dc:creator":["Cheung, Stephanie, S.M. Massachusetts Institute of Technology"],"dc:date.accessioned":["2014-05-23T19:35:12Z"],"dc:date.available":["2014-05-23T19:35:12Z"],"dc:date.issued":["2014"],"dc:description":["Thesis: S.M., Massachusetts Institute of Technology, Department of Chemistry, 2014.","Cataloged from PDF version of thesis.","Includes bibliographical references."],"dc:description.abstract":["One of the most remarkable ideas in modem biology is that organization of multicellular life is orchestrated by a relatively small repertoire of signaling molecules, which mediate communication between cells. Breakdown of these communication pathways can have profound consequences, leading to a multiplicity of developmental defects and disease states. In particular, the ErbB family of receptors and ligands regulate key cellular processes such as proliferation, differentiation, and apoptosis during embryonic development, cellular homeostasis, and tumorigenesis. The generality of the ErbB-network has made it one of the most well-studied cell signaling systems. However, traditional methods used to study cellular signaling either fail to capture the dynamic nature of signaling networks or to lack the ability to quantify native signaling components. To further our understanding of the signaling processes that govern cell fate and tissue health, novel non-invasive techniques must be developed to quantitatively track native protein analytes in live cells. Herein approaches toward the development of a set novel fluorogenic biosensors capable of detecting native ErbB-ligands are reported. Using yeast surface display, two libraries of protein-binding scaffolds were engineered to bind selectively to human EGF and human betacellulin with low nM KD. Bio-orthogonal conjugation of these protein scaffolds to 4-DMN, a solvatochromic fluorophore, afforded a biosensor that exhibit a 3-fold fluorescence increase upon binding human EGF. Efforts to improve the fluorescent signal via alternative labeling strategies are also reported."],"dc:description.degree":["S.M."],"dc:identifier.uri":["http://hdl.handle.net/1721.1/87473"],"dc:language.iso":["eng"],"dc:publisher":["Massachusetts Institute of Technology"],"dc:rights":["M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission."],"dc:rights.uri":["http://dspace.mit.edu/handle/1721.1/7582"],"dc:subject":["Chemistry."],"dc:title":["Approaches towards development of novel fluorogenic biosensors for detection of small protein analytes"],"dc:type":["Thesis"]},"updated_at":"2026-07-22T22:22:16Z"}