Valet Parking for Protein Ion Charge State Concentration: Ion/Molecule Reactions in Linear Ion Traps.


Journal

Analytical chemistry
ISSN: 1520-6882
Titre abrégé: Anal Chem
Pays: United States
ID NLM: 0370536

Informations de publication

Date de publication:
07 04 2020
Historique:
pubmed: 27 2 2020
medline: 21 1 2021
entrez: 27 2 2020
Statut: ppublish

Résumé

There are several analytical applications in which it is desirable to concentrate analyte ions generated over a range of charge states into a single charge state. This has been demonstrated in the gas phase via ion/ion reactions in conjunction with a technique termed ion parking, which can be implemented in electrodynamic ion traps. Ion parking depends upon the selective inhibition of the reaction of a selected charge state or charge states. In this work, we demonstrate a similar charge state concentration effect using ion/molecule reactions rather than ion/ion reactions. The rates of ion/molecule reactions cannot be affected in the manner used in conventional ion parking. Rather, to inhibit the progression of ion/molecule proton transfer reactions, the product ions must be removed from the reaction cell as they are formed and transferred to an ion trap where no reactions occur. This is accomplished here with mass-selective axial ejection (MSAE) from one linear ion trap to another. The application of MSAE to inhibit ion/molecule reactions is referred to as "valet parking" as it entails the transport of the ions of interest to a remote location for storage. Valet parking is demonstrated using model proteins to concentrate ion signal dispersed over multiple charge states into largely one charge state. Additionally, it has been applied to a simple two-protein mixture of cytochrome

Identifiants

pubmed: 32100997
doi: 10.1021/acs.analchem.0c00146
pmc: PMC7145756
mid: NIHMS1570159
doi:

Substances chimiques

Myoglobin 0
Proteins 0
Cytochromes c 9007-43-6

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5419-5425

Subventions

Organisme : NIGMS NIH HHS
ID : R37 GM045372
Pays : United States

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Auteurs

David J Foreman (DJ)

Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-2084, United States.

Jay S Bhanot (JS)

Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-2084, United States.

Kenneth W Lee (KW)

Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-2084, United States.

Scott A McLuckey (SA)

Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-2084, United States.

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Classifications MeSH