Repozytorium

A mechanistic study on the fragmentation of peptide-derived Amadori products.

Autorzy

Piotr Stefanowicz

Katarzyna Kapczyńska

Mariusz Jaremko

Łukasz Jaremko

Zbigniew Szewczuk

Rok wydania

2009

Czasopismo

Journal of Mass Spectrometry

Numer woluminu

44

Strony

1500-1508

DOI

10.1002/jms.1639

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

Gas phase fragmentation of peptide-derived Amadori products was investigated using synthetic compounds regioselectively deuterated as well as labeled with 18O at aminofructose moiety. The eliminated molecule CH2O contains exclusively protons attached to carbon C6 of the aminofructose moiety. The hydrogen atoms connected with the carbon C1 of the aminofructose moiety are partially eliminated as a component of water molecules during the dehydration process and partially dislocated within the fragmented peptide molecule. The labeled oxygen atom attached to the carbon C2 is eliminated in 100% along with the first loss of water. The MS3 experiments revealed that the product ion formed by triple dehydration of the Amadori product does not eliminate the formaldehyde molecule. On the basis of these observations we proposed a hypothetical mechanism of Amadori products' fragmentation.

Adres publiczny

https://doi.org/10.1002/jms.1639

Strona internetowa wydawcy

onlinelibrary.wiley.com

Podobne publikacje
2005

The synthesis of peptide derived Amadori products on a solid support.

Kapczyńska Katarzyna, Stefanowicz Piotr, Szewczuk Zbigniew

2007

A new procedure for the synthesis of peptide-derived Amadori products on a solid support.

Stefanowicz Piotr, Kapczyńska Katarzyna, Kluczyk Alicja, Szewczuk Zbigniew

2007

The studies on the optimization of the solid phase synthesis of peptide-derived Amadori products.

Stefanowicz Piotr, Kapczyńska Katarzyna, Brunatna Monika, Szewczuk Zbigniew