- AutorIn
- Johann Sajapin Chair of Food Chemistry, Technische Universität Dresden
- Annemarie KulasChair of Food Chemistry, Technische Universität Dresden
- Michael HellwigChair of Food Chemistry, Technische Universität Dresden, Dresden#Chair of Special Food Chemistry, Technische Universität Dresden
- Titel
- Methionine-associated peptide α-amidation is directed both to the N- and the C-terminal amino acids
- Zitierfähige Url:
- https://nbn-resolving.org/urn:nbn:de:bsz:14-qucosa2-910108
- Quellenangabe
- Journal of peptide science
Erscheinungsjahr: 2022
Jahrgang: 28
Heft: 11
E-ISSN: 1099-1387
Artikelnummer: e3429 - Erstveröffentlichung
- 2022
- Abstract (EN)
- Peptide-bound methionine may transfer oxidative damage from the thioether side chain to the peptide backbone, catalyzing decomposition in general and α-amidation in particular. In the present study, we focused on the reactivity and reaction pathways of peptides. We synthesized model peptides comprising methionine or not and investigated their overall tendency towards decomposition and formation of specific products under conditions mimicking the cooking process at 100°C in buffered solution (pH 6.0) in the presence of redox-active substances such as transition metal ions and reductones. Peptides containing methionine were more susceptible to α-amidation under all oxidative conditions, and the products of N-terminus-directed α-amidation were quantified. Exemplarily, after incubation in the presence of cupric sulfate, about 2.0 mol-% of the overall decomposition of Z-glycylmethionylglycine accounted for the formation of Z-glycinamide, whereas it was below 0.1 mol-% for Z-glycylalanylglycine. Surprisingly and different from previous observations, C-terminus-directed α-amidation was observed for the first time. From Z-glycylmethionylglycine, the respective products were formed in higher amounts than the N-terminus-directed α-amidation product Z-glycinamide under all applied oxidation conditions. The preference of electron transfer from the amino nitrogen bound in the peptide bond directed to the C-terminus may be ascribed to a sterically less demanding hexagonal 3-electron-2-center intermediate during methionine-catalyzed α-amidation.
- Andere Ausgabe
- Link zum Artikel der zuerst in der Zeitschrift „Journal of peptide science” bei Wiley erschienen ist.
DOI: 10.1002/psc.3429 - Freie Schlagwörter (DE)
- Rückgratspaltung, Katalyse, Methionin, Proteinoxidation, reaktive Sauerstoffspezies, α-Amidierung
- Freie Schlagwörter (EN)
- backbone cleavage, catalysis, methionine, protein oxidation, reactive oxygen species, α-amidation
- Klassifikation (DDC)
- 570
- 540
- Verlag
- Wiley, New York, NY [u.a.]
- Förder- / Projektangaben
- Deutsche Forschungsgemeinschaft (DFG)
ID: HE 7681/1-1 - Version / Begutachtungsstatus
- publizierte Version / Verlagsversion
- URN Qucosa
- urn:nbn:de:bsz:14-qucosa2-910108
- Veröffentlichungsdatum Qucosa
- 22.05.2024
- Dokumenttyp
- Artikel
- Sprache des Dokumentes
- Englisch
- Lizenz / Rechtehinweis
CC BY-NC-ND 4.0