{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/87884"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/87884","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Convergent Site-Selective Carbohydrate-Peptide Ligations With Dehydroalanine and Aziridine -2 -Carboxylic Acid-Containing Peptides","abstract":"The development of two convergent strategies for site-selective peptide modification and their application to the preparation of alpha-thio analogs of mucin related glycoconjugates is described. Chemoselectivity in these reactions was realized through the incorporation of dehydroalanine and aziridine-2-carboxylic acid residues into peptides and subsequent conjugation of the resulting peptide electrophiles with various thiols. Oligosaccharides incorporating a suitable anomeric thio-functionality were prepared via dehydrative glycosylation and glycolamide-auxiliary controlled sialylation reactions. The efficiency of the dehydroalanine ligation approach was demonstrated by the preparation of thio-isosteres of the four tumor-associated carbohydrate antigens, T N, T, STN, and 2,6-ST, as a pair of diastereoisomers at the newly formed cysteine stereocenter. This 1,4-conjugate addition ligation proceeded in high yield and with retention of alpha-anomeric configuration of the carbohydrate donor. In addition, site- and stereoselective peptide modification of aziridine-2-carboxylic acid-containing peptides was achieved. A solid-phase peptide synthesis methodology that allows for the rapid generation of peptides incorporating the aziridine residue was developed. The resulting peptides were conjugated with various thiol nucleophiles, such as anomeric carbohydrate thiols, farnesyl thiol, and biochemical tags, both in solution and on solid support. This ligation proceeds with the retention of the anomeric configuration of carbohydrate nucleophiles, and (R) configuration at the alpha-carbon of the newly formed cysteine derivative. This strategy, combined with native chemical ligation, provided convergent and rapid access to complex glycoconjugates. The developed convergent peptide modification approaches should allow for the construction of a variety of glycopeptide and lipopeptide conjugates for biological evaluations.","abstract_html":"The development of two convergent strategies for site-selective peptide modification and their application to the preparation of alpha-thio analogs of mucin related glycoconjugates is described. Chemoselectivity in these reactions was realized through the incorporation of dehydroalanine and aziridine-2-carboxylic acid residues into peptides and subsequent conjugation of the resulting peptide electrophiles with various thiols. Oligosaccharides incorporating a suitable anomeric thio-functionality were prepared via dehydrative glycosylation and glycolamide-auxiliary controlled sialylation reactions. The efficiency of the dehydroalanine ligation approach was demonstrated by the preparation of thio-isosteres of the four tumor-associated carbohydrate antigens, T N, T, STN, and 2,6-ST, as a pair of diastereoisomers at the newly formed cysteine stereocenter. This 1,4-conjugate addition ligation proceeded in high yield and with retention of alpha-anomeric configuration of the carbohydrate donor. In addition, site- and stereoselective peptide modification of aziridine-2-carboxylic acid-containing peptides was achieved. A solid-phase peptide synthesis methodology that allows for the rapid generation of peptides incorporating the aziridine residue was developed. The resulting peptides were conjugated with various thiol nucleophiles, such as anomeric carbohydrate thiols, farnesyl thiol, and biochemical tags, both in solution and on solid support. This ligation proceeds with the retention of the anomeric configuration of carbohydrate nucleophiles, and (R) configuration at the alpha-carbon of the newly formed cysteine derivative. This strategy, combined with native chemical ligation, provided convergent and rapid access to complex glycoconjugates. The developed convergent peptide modification approaches should allow for the construction of a variety of glycopeptide and lipopeptide conjugates for biological evaluations.","abstract_has_math":false,"creators":["Galonic, Danica"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":null,"degree_department":null,"school":null,"contributors":["van der Donk, Wilfred A.","Gin, David Y."],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2015,"date_issued":"2015-09-28T21:57:26Z","date_published":"2015-09-28T21:57:26Z","updated_at":"2026-07-22T22:26:31Z","subjects":["Chemistry, Organic"],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["(MiAaPQ)AAI3198998"],"render_values":[{"text":"(MiAaPQ)AAI3198998","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/2142/87884","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["van der Donk, Wilfred A.","Gin, David Y."]},{"key":"dc:creator","label":"Author","values":["Galonic, Danica"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2015-09-28T21:57:26Z","10000-01-01","2005"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"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":["Chemistry, Organic"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/87884","(MiAaPQ)AAI3198998"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["The development of two convergent strategies for site-selective peptide modification and their application to the preparation of alpha-thio analogs of mucin related glycoconjugates is described. Chemoselectivity in these reactions was realized through the incorporation of dehydroalanine and aziridine-2-carboxylic acid residues into peptides and subsequent conjugation of the resulting peptide electrophiles with various thiols. Oligosaccharides incorporating a suitable anomeric thio-functionality were prepared via dehydrative glycosylation and glycolamide-auxiliary controlled sialylation reactions. The efficiency of the dehydroalanine ligation approach was demonstrated by the preparation of thio-isosteres of the four tumor-associated carbohydrate antigens, T N, T, STN, and 2,6-ST, as a pair of diastereoisomers at the newly formed cysteine stereocenter. This 1,4-conjugate addition ligation proceeded in high yield and with retention of alpha-anomeric configuration of the carbohydrate donor. In addition, site- and stereoselective peptide modification of aziridine-2-carboxylic acid-containing peptides was achieved. A solid-phase peptide synthesis methodology that allows for the rapid generation of peptides incorporating the aziridine residue was developed. The resulting peptides were conjugated with various thiol nucleophiles, such as anomeric carbohydrate thiols, farnesyl thiol, and biochemical tags, both in solution and on solid support. This ligation proceeds with the retention of the anomeric configuration of carbohydrate nucleophiles, and (R) configuration at the alpha-carbon of the newly formed cysteine derivative. This strategy, combined with native chemical ligation, provided convergent and rapid access to complex glycoconjugates. The developed convergent peptide modification approaches should allow for the construction of a variety of glycopeptide and lipopeptide conjugates for biological evaluations.","Made available in DSpace on 2015-09-28T21:57:26Z (GMT). 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Chemoselectivity in these reactions was realized through the incorporation of dehydroalanine and aziridine-2-carboxylic acid residues into peptides and subsequent conjugation of the resulting peptide electrophiles with various thiols. Oligosaccharides incorporating a suitable anomeric thio-functionality were prepared via dehydrative glycosylation and glycolamide-auxiliary controlled sialylation reactions. The efficiency of the dehydroalanine ligation approach was demonstrated by the preparation of thio-isosteres of the four tumor-associated carbohydrate antigens, T N, T, STN, and 2,6-ST, as a pair of diastereoisomers at the newly formed cysteine stereocenter. This 1,4-conjugate addition ligation proceeded in high yield and with retention of alpha-anomeric configuration of the carbohydrate donor. In addition, site- and stereoselective peptide modification of aziridine-2-carboxylic acid-containing peptides was achieved. A solid-phase peptide synthesis methodology that allows for the rapid generation of peptides incorporating the aziridine residue was developed. The resulting peptides were conjugated with various thiol nucleophiles, such as anomeric carbohydrate thiols, farnesyl thiol, and biochemical tags, both in solution and on solid support. This ligation proceeds with the retention of the anomeric configuration of carbohydrate nucleophiles, and (R) configuration at the alpha-carbon of the newly formed cysteine derivative. This strategy, combined with native chemical ligation, provided convergent and rapid access to complex glycoconjugates. The developed convergent peptide modification approaches should allow for the construction of a variety of glycopeptide and lipopeptide conjugates for biological evaluations.","Made available in DSpace on 2015-09-28T21:57:26Z (GMT). No. of bitstreams: 2 license.txt: 4848 bytes, checksum: 96035ab3f5e1c23cc7138a224ce498bd (MD5) 3198998.pdf: 5422336 bytes, checksum: a484015f91f51c72bcd56d82d9a63fa9 (MD5) Previous issue date: 2005","Embargo set by: Seth Robbins for item 89165 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","U of I Only","222 p.","Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2005."],"dc:identifier":["http://hdl.handle.net/2142/87884","(MiAaPQ)AAI3198998"],"dc:language":["eng"],"dc:subject":["Chemistry, Organic"],"dc:title":["Convergent Site-Selective Carbohydrate-Peptide Ligations With Dehydroalanine and Aziridine -2 -Carboxylic Acid-Containing Peptides"],"dc:type":["text"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Ph.D."],"thesis:institution_name":["University of Illinois at Urbana-Champaign"]},"updated_at":"2026-07-22T22:26:31Z"}