{"id":{"repo_id":"purdue-thes","oai_identifier":"oai:docs.lib.purdue.edu:open_access_dissertations-2610"},"canonical_url":"https://search.dev.ndltd.org/etd/purdue-thes/oai:docs.lib.purdue.edu:open_access_dissertations-2610","repository":{"repo_id":"purdue-thes","name":"Purdue University","base_url":"https://docs.lib.purdue.edu/do/oai/"},"display":{"title":"The Gas-Phase Oxidation of Cationic Bioanalytes via Ion/Ion Reactions","abstract":"Several solution-phase derivatizations have recently been implemented in the gas-phase through the interaction between oppositely charged ions, viz., ion/ion reactions. The work presented here primarily focuses on the oxidation of bioanalytes via ion/ion reactions with periodate and persulfate anions. Methionine and tryptophan residues in simple polypeptides are selectively oxidized upon ion/ion reactions with periodate anion. The oxidative labeling of disulfide bonds is performed via ion/ion reactions and is used to identify intermolecularly disulfide-linked peptides and further probe their primary structure. Non-modified, non-disulfide linked peptides lacking easily oxidized residues (i.e., methionine and tryptophan) can also undergo oxidation. Peptides containing neutral basic sites undergo oxidation upon ion/ion reactions with periodate anion to various forms, including the [M+H+O]+,[M-H]+, and [M-H-NH3]+ species. Furthermore, persulfate anion is a stronger oxidizing reagent than periodate and increases the amount of oxidation observed with these less-readily oxidized residues. Persulfate anion and its derivatives, sulfate radical anion and peroxymonosulfate anion are capable of generating a variety of oxidation products, including the [M+H+O]+, [M-H]+, and M+• species.","abstract_html":"Several solution-phase derivatizations have recently been implemented in the gas-phase through the interaction between oppositely charged ions, viz., ion/ion reactions. The work presented here primarily focuses on the oxidation of bioanalytes via ion/ion reactions with periodate and persulfate anions. Methionine and tryptophan residues in simple polypeptides are selectively oxidized upon ion/ion reactions with periodate anion. The oxidative labeling of disulfide bonds is performed via ion/ion reactions and is used to identify intermolecularly disulfide-linked peptides and further probe their primary structure. Non-modified, non-disulfide linked peptides lacking easily oxidized residues (i.e., methionine and tryptophan) can also undergo oxidation. Peptides containing neutral basic sites undergo oxidation upon ion/ion reactions with periodate anion to various forms, including the [M+H+O]+,[M-H]+, and [M-H-NH3]+ species. Furthermore, persulfate anion is a stronger oxidizing reagent than periodate and increases the amount of oxidation observed with these less-readily oxidized residues. Persulfate anion and its derivatives, sulfate radical anion and peroxymonosulfate anion are capable of generating a variety of oxidation products, including the [M+H+O]+, [M-H]+, and M+• species.","abstract_has_math":false,"creators":["Pilo, Alice Lindsay"],"institution":null,"degree_name":"Doctor of Philosophy (PhD)","degree_level":"Dissertation","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":["Scott A McLuckey","Mary J Wirth","Marcy H Towns","Paul Wenthold"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2016,"date_issued":"2016-01-01T08:00:00Z","date_published":"2016-01-01T08:00:00Z","updated_at":"2026-07-24T03:54:38Z","subjects":["Dehydroalanine","Ion/Ion Reactions","Oxidation","Radical Cations","Tandem Mass Spectrometry"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://docs.lib.purdue.edu/open_access_dissertations/1394","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Scott A McLuckey","Mary J Wirth","Marcy H Towns","Paul Wenthold"]},{"key":"dc:creator","label":"Author","values":["Pilo, Alice Lindsay"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Doctor of Philosophy (PhD)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Dehydroalanine","Ion/Ion Reactions","Oxidation","Radical Cations","Tandem Mass Spectrometry"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://docs.lib.purdue.edu/open_access_dissertations/1394"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Several solution-phase derivatizations have recently been implemented in the gas-phase through the interaction between oppositely charged ions, viz., ion/ion reactions. The work presented here primarily focuses on the oxidation of bioanalytes via ion/ion reactions with periodate and persulfate anions. Methionine and tryptophan residues in simple polypeptides are selectively oxidized upon ion/ion reactions with periodate anion. The oxidative labeling of disulfide bonds is performed via ion/ion reactions and is used to identify intermolecularly disulfide-linked peptides and further probe their primary structure. Non-modified, non-disulfide linked peptides lacking easily oxidized residues (i.e., methionine and tryptophan) can also undergo oxidation. Peptides containing neutral basic sites undergo oxidation upon ion/ion reactions with periodate anion to various forms, including the [M+H+O]+,[M-H]+, and [M-H-NH3]+ species. Furthermore, persulfate anion is a stronger oxidizing reagent than periodate and increases the amount of oxidation observed with these less-readily oxidized residues. Persulfate anion and its derivatives, sulfate radical anion and peroxymonosulfate anion are capable of generating a variety of oxidation products, including the [M+H+O]+, [M-H]+, and M+• species."]},{"key":"dc:title","label":"Title","values":["The Gas-Phase Oxidation of Cationic Bioanalytes via Ion/Ion Reactions"]}]}],"canonical_facts":{"dc:contributor":["Scott A McLuckey","Mary J Wirth","Marcy H Towns","Paul Wenthold"],"dc:creator":["Pilo, Alice Lindsay"],"dc:description.abstract":["Several solution-phase derivatizations have recently been implemented in the gas-phase through the interaction between oppositely charged ions, viz., ion/ion reactions. The work presented here primarily focuses on the oxidation of bioanalytes via ion/ion reactions with periodate and persulfate anions. Methionine and tryptophan residues in simple polypeptides are selectively oxidized upon ion/ion reactions with periodate anion. The oxidative labeling of disulfide bonds is performed via ion/ion reactions and is used to identify intermolecularly disulfide-linked peptides and further probe their primary structure. Non-modified, non-disulfide linked peptides lacking easily oxidized residues (i.e., methionine and tryptophan) can also undergo oxidation. Peptides containing neutral basic sites undergo oxidation upon ion/ion reactions with periodate anion to various forms, including the [M+H+O]+,[M-H]+, and [M-H-NH3]+ species. Furthermore, persulfate anion is a stronger oxidizing reagent than periodate and increases the amount of oxidation observed with these less-readily oxidized residues. Persulfate anion and its derivatives, sulfate radical anion and peroxymonosulfate anion are capable of generating a variety of oxidation products, including the [M+H+O]+, [M-H]+, and M+• species."],"dc:identifier":["https://docs.lib.purdue.edu/open_access_dissertations/1394"],"dc:subject":["Dehydroalanine","Ion/Ion Reactions","Oxidation","Radical Cations","Tandem Mass Spectrometry"],"dc:title":["The Gas-Phase Oxidation of Cationic Bioanalytes via Ion/Ion Reactions"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Doctor of Philosophy (PhD)"]},"updated_at":"2026-07-24T03:54:38Z"}