Article (Scientific journals)
Cyclic Peptide Protomer Detection in the Gas Phase: Impact on CCS Measurement and Fragmentation Patterns.
Mc Cann, Andréa; Kune, Christopher; Massonnet, Philippe et al.
2022In Journal of the American Society for Mass Spectrometry, 33 (5), p. 851-858
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Keywords :
breakdown curves; cyclic lipopeptides; ion mobility; protomers; structures; Lipopeptides; Protons; Molecular Conformation; Protein Subunits/chemistry; Cyclic peptides; Gas-phases; Ionization modes; Surfactins; Structural Biology; Spectroscopy; Prototropic tautomers; tautomerization
Abstract :
[en] With the recent improvements in ion mobility resolution, it is now possible to separate small protomeric tautomers, called protomers. In larger molecules above 1000 Da such as peptides, a few studies suggest that protomers do exist as well and may contribute to their gas-phase conformational heterogeneity. In this work, we observed a CCS distribution that can be explained by the presence of protomers of surfactin, a small lipopeptide with no basic site. Following preliminary density functional theoretical calculations, several protonation sites in the gas phase were energetically favorable in positive ionization mode. Experimentally, at least three near-resolved IM peaks were observed in positive ionization mode, while only one was detected in negative ionization mode. These results were in good agreement with the DFT predictions. CID breakdown curve analysis after IM separation showed different inflection points (CE50) suggesting that different intramolecular interactions were implied in the stabilization of the structures of surfactin. The fragment ratio observed after collision-induced fragmentation was also different, suggesting different ring-opening localizations. All these observations support the presence of protomers on the cyclic peptide moieties of the surfactin. These data strongly suggest that protomeric tautomerism can still be observed on molecules above 1000 Da if the IM resolving power is sufficient. It also supports that the proton localization involves a change in the 3D structure that can affect the experimental CCS and the fragmentation channels of such peptides.
Disciplines :
Chemistry
Author, co-author :
Mc Cann, Andréa   ;  Université de Liège - ULiège > Département de chimie (sciences) > Laboratoire de spectrométrie de masse (L.S.M.)
Kune, Christopher   ;  Université de Liège - ULiège > Molecular Systems (MolSys)
Massonnet, Philippe  ;  Université de Liège - ULiège > Département de chimie (sciences) > Chimie biologique ; Maastricht Multimodal Molecular Imaging (M4I) Institute, Division of Imaging Mass Spectrometry, 6229ER Maastricht, Limburg, The Netherlands
Far, Johann  ;  Université de Liège - ULiège > Molecular Systems (MolSys)
Ongena, Marc ;  Université de Liège - ULiège > Département GxABT > Microbial technologies
Eppe, Gauthier  ;  Université de Liège - ULiège > Molecular Systems (MolSys)
Quinton, Loïc  ;  Université de Liège - ULiège > Molecular Systems (MolSys)
De Pauw, Edwin  ;  Université de Liège - ULiège > Département de chimie (sciences)
 These authors have contributed equally to this work.
Language :
English
Title :
Cyclic Peptide Protomer Detection in the Gas Phase: Impact on CCS Measurement and Fragmentation Patterns.
Publication date :
04 May 2022
Journal title :
Journal of the American Society for Mass Spectrometry
ISSN :
1044-0305
eISSN :
1879-1123
Publisher :
American Chemical Society, United States
Volume :
33
Issue :
5
Pages :
851-858
Peer reviewed :
Peer Reviewed verified by ORBi
Funders :
F.R.S.-FNRS - Fonds de la Recherche Scientifique [BE]
Funding text :
A. McCann and C. Kune thank the Excellence Of Science (EOS) Program (Rhizoclip EOS2018000802) of the FNRS F.R.S for financial support. The authors want to thank the TCP group of the University of Liège, especially prof. F. Remacle, for sharing calculation servers allowing the modeling of lipopeptides. Finally, the authors would like to thank D. McCann for his kind review and suggestions.
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since 26 September 2022

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