Probing Structural Information of Gas-Phase Peptides by Near-Edge X-ray Absorption Mass Spectrometry.
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:
03 Mar 2021
03 Mar 2021
Historique:
pubmed:
13
2
2021
medline:
27
10
2021
entrez:
12
2
2021
Statut:
ppublish
Résumé
Near-edge X-ray absorption mass spectrometry (NEXAMS) is an action-spectroscopy technique of growing interest for investigations into the spatial and electronic structure of biomolecules. It has been used successfully to give insights into different aspects of the photodissociation of peptides and to probe the conformation of proteins. It is a current question whether the fragmentation pathways are sensitive toward effects of conformational isomerism, tautomerism, and intramolecular interactions in gas-phase peptides. To address this issue, we studied the cationic fragments of cryogenically cooled gas-phase leucine enkephalin ([LeuEnk+H]
Identifiants
pubmed: 33573373
doi: 10.1021/jasms.0c00390
doi:
Substances chimiques
Enkephalins
0
Peptides
0
Enkephalin, Methionine
58569-55-4
Enkephalin, Leucine
58822-25-6
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM