Digital Quadrupole Isolation and Electron Capture Dissociation on an Extended Mass Range Q-TOF Provides Sequence and Structure Information on Proteins and Protein Complexes.
charge reduction
digital quadrupole
electron capture dissociation
native mass spectrometry
protein structure
Journal
Journal of the American Society for Mass Spectrometry
ISSN: 1879-1123
Titre abrégé: J Am Soc Mass Spectrom
Pays: United States
ID NLM: 9010412
Informations de publication
Date de publication:
02 Aug 2023
02 Aug 2023
Historique:
pmc-release:
02
08
2024
medline:
3
8
2023
pubmed:
18
7
2023
entrez:
18
7
2023
Statut:
ppublish
Résumé
Electron capture dissociation (ECD) is now a well-established method for sequencing peptides and performing top-down analysis on proteins of less than 30 kDa, and there is growing interest in using this approach for studies of larger proteins and protein complexes. Although much progress on ECD has been made over the past few decades, establishing methods for obtaining informative spectra still poses a significant challenge. Here we describe how digital quadrupole (DigiQ) ion isolation can be used for the mass selection of single charge states of proteins and protein complexes prior to undergoing ECD and/or charge reduction. First, we demonstrate that the DigiQ can isolate single charge states of monomeric proteins such as ubiquitin (8.6 kDa) and charge states of large protein complexes such as pyruvate kinase (234 kDa) using a hybrid quadrupole-TOF-MS (Agilent extended
Identifiants
pubmed: 37463113
doi: 10.1021/jasms.3c00184
pmc: PMC10496594
mid: NIHMS1916109
doi:
Substances chimiques
Streptavidin
9013-20-1
Biotin
6SO6U10H04
Proteins
0
Ubiquitin
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1753-1760Subventions
Organisme : NIGMS NIH HHS
ID : P41 GM128577
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM138863
Pays : United States
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