Gas-phase ion/ion chemistry involves the interaction of oppositely charged ions inside of the mass spectrometer. During this gas-phase chemistry, particle transfer (i.e., proton and electron) or synthesis can occur at rapid reaction rates. Particle transfer represents a mature area of ion/ion chemistry, while selective covalent modification represents a fairly new area of gas-phase chemistry. Gas-phase covalent chemistry is based on traditional solution phase organic chemistry.
The work demonstrated in this dissertation greatly involves gas-phase covalent and non-covalent Schiff base chemistry on peptide and protein ions. The reagent dianion, 4-formyl 1,3-benzene disulfonic acid, has been used to covalently modify unprotonated primary amines present in peptide and protein ions. In addition, strong non-covalent interactions have also been observed with arginine-containing peptides ions. Studies of their dissociation behavior as well as the nature of their interaction (i.e., covalent versus non-covalent) have been investigated. Application of this Schiff base ion/ion chemistry has been demonstrated on matrix assisted laser desorption/ionization (MALDI)-derived peptide ions. Such Schiff base ion/ion chemistry, whether electrospray or MALDI-derived, can produce complementary or even an increase in structural information. Multiple covalent modifications within one ion/ion encounter have been demonstrated on peptide and protein cations via Schiff base cluster anions. This dissertation also highlights the gas-phase transformation of phosphatidylcholine cations into demethylated phosphatidylcholine anions, which provides an increase in structural information upon activation. As a whole, gas-phase covalent and non-covalent ion/ion chemistry represents a promising new area for identifying and characterizing biological analytes.
","abstract_html":"<p>Gas-phase ion/ion chemistry involves the interaction of oppositely charged ions inside of the mass spectrometer. During this gas-phase chemistry, particle transfer (i.e., proton and electron) or synthesis can occur at rapid reaction rates. Particle transfer represents a mature area of ion/ion chemistry, while selective covalent modification represents a fairly new area of gas-phase chemistry. Gas-phase covalent chemistry is based on traditional solution phase organic chemistry.</p> <p>The work demonstrated in this dissertation greatly involves gas-phase covalent and non-covalent Schiff base chemistry on peptide and protein ions. The reagent dianion, 4-formyl 1,3-benzene disulfonic acid, has been used to covalently modify unprotonated primary amines present in peptide and protein ions. In addition, strong non-covalent interactions have also been observed with arginine-containing peptides ions. Studies of their dissociation behavior as well as the nature of their interaction (i.e., covalent versus non-covalent) have been investigated. Application of this Schiff base ion/ion chemistry has been demonstrated on matrix assisted laser desorption/ionization (MALDI)-derived peptide ions. Such Schiff base ion/ion chemistry, whether electrospray or MALDI-derived, can produce complementary or even an increase in structural information. Multiple covalent modifications within one ion/ion encounter have been demonstrated on peptide and protein cations via Schiff base cluster anions. This dissertation also highlights the gas-phase transformation of phosphatidylcholine cations into demethylated phosphatidylcholine anions, which provides an increase in structural information upon activation. As a whole, gas-phase covalent and non-covalent ion/ion chemistry represents a promising new area for identifying and characterizing biological analytes.</p>","abstract_has_math":false,"creators":["Stutzman, John Robert"],"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","Mingji Dai","David H. Thompson"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2013,"date_issued":"2013-10-01T07:00:00Z","date_published":"2013-10-01T07:00:00Z","updated_at":"2026-07-24T03:53:11Z","subjects":["pure sciences","gas phase ion chemistry","mass spectrometry","covalent ions","non-covalent ions","macromolecules","Biochemistry","Chemistry","Physical Chemistry"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://docs.lib.purdue.edu/open_access_dissertations/46","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","Mingji Dai","David H. Thompson"]},{"key":"dc:creator","label":"Author","values":["Stutzman, John Robert"]}]},{"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":["pure sciences","gas phase ion chemistry","mass spectrometry","covalent ions","non-covalent ions","macromolecules","Biochemistry","Chemistry","Physical Chemistry"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://docs.lib.purdue.edu/open_access_dissertations/46"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Gas-phase ion/ion chemistry involves the interaction of oppositely charged ions inside of the mass spectrometer. During this gas-phase chemistry, particle transfer (i.e., proton and electron) or synthesis can occur at rapid reaction rates. Particle transfer represents a mature area of ion/ion chemistry, while selective covalent modification represents a fairly new area of gas-phase chemistry. Gas-phase covalent chemistry is based on traditional solution phase organic chemistry.
The work demonstrated in this dissertation greatly involves gas-phase covalent and non-covalent Schiff base chemistry on peptide and protein ions. The reagent dianion, 4-formyl 1,3-benzene disulfonic acid, has been used to covalently modify unprotonated primary amines present in peptide and protein ions. In addition, strong non-covalent interactions have also been observed with arginine-containing peptides ions. Studies of their dissociation behavior as well as the nature of their interaction (i.e., covalent versus non-covalent) have been investigated. Application of this Schiff base ion/ion chemistry has been demonstrated on matrix assisted laser desorption/ionization (MALDI)-derived peptide ions. Such Schiff base ion/ion chemistry, whether electrospray or MALDI-derived, can produce complementary or even an increase in structural information. Multiple covalent modifications within one ion/ion encounter have been demonstrated on peptide and protein cations via Schiff base cluster anions. This dissertation also highlights the gas-phase transformation of phosphatidylcholine cations into demethylated phosphatidylcholine anions, which provides an increase in structural information upon activation. As a whole, gas-phase covalent and non-covalent ion/ion chemistry represents a promising new area for identifying and characterizing biological analytes.
"]},{"key":"dc:title","label":"Title","values":["Gas-Phase Covalent And Non-Covalent Ion/ion Chemistry Of Biological Macromolecules"]}]}],"canonical_facts":{"dc:contributor":["Scott A. McLuckey","Mary J. Wirth","Mingji Dai","David H. Thompson"],"dc:creator":["Stutzman, John Robert"],"dc:description.abstract":["Gas-phase ion/ion chemistry involves the interaction of oppositely charged ions inside of the mass spectrometer. During this gas-phase chemistry, particle transfer (i.e., proton and electron) or synthesis can occur at rapid reaction rates. Particle transfer represents a mature area of ion/ion chemistry, while selective covalent modification represents a fairly new area of gas-phase chemistry. Gas-phase covalent chemistry is based on traditional solution phase organic chemistry.
The work demonstrated in this dissertation greatly involves gas-phase covalent and non-covalent Schiff base chemistry on peptide and protein ions. The reagent dianion, 4-formyl 1,3-benzene disulfonic acid, has been used to covalently modify unprotonated primary amines present in peptide and protein ions. In addition, strong non-covalent interactions have also been observed with arginine-containing peptides ions. Studies of their dissociation behavior as well as the nature of their interaction (i.e., covalent versus non-covalent) have been investigated. Application of this Schiff base ion/ion chemistry has been demonstrated on matrix assisted laser desorption/ionization (MALDI)-derived peptide ions. Such Schiff base ion/ion chemistry, whether electrospray or MALDI-derived, can produce complementary or even an increase in structural information. Multiple covalent modifications within one ion/ion encounter have been demonstrated on peptide and protein cations via Schiff base cluster anions. This dissertation also highlights the gas-phase transformation of phosphatidylcholine cations into demethylated phosphatidylcholine anions, which provides an increase in structural information upon activation. As a whole, gas-phase covalent and non-covalent ion/ion chemistry represents a promising new area for identifying and characterizing biological analytes.
"],"dc:identifier":["https://docs.lib.purdue.edu/open_access_dissertations/46"],"dc:subject":["pure sciences","gas phase ion chemistry","mass spectrometry","covalent ions","non-covalent ions","macromolecules","Biochemistry","Chemistry","Physical Chemistry"],"dc:title":["Gas-Phase Covalent And Non-Covalent Ion/ion Chemistry Of Biological Macromolecules"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Doctor of Philosophy (PhD)"]},"updated_at":"2026-07-24T03:53:11Z"}