The b1 ion derived from methionine is a stable species
β Scribed by Ya-Ping Tu; Alex. G. Harrison
- Book ID
- 101236567
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 57 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0951-4198
No coin nor oath required. For personal study only.
β¦ Synopsis
Unimolecular fragmentation of the MH ions of a number of methionine derivatives such as H-Met-OMe, H-Met-b-naphthylamide, H-Met-Gly-OH, H-Met-Ala-OH and H-Met-Phe-OH results in formation of the methionine b 1 ion (m/z 132) in significant yields. Since a-aminoacylium ions are generally unstable and not observed, it is proposed that the stable form of the b 1 ion from these methionine derivatives is methylcationated a-amino-g-thiobutyrolactone. Under low-energy collision-induced dissociation conditions this b 1 ion readily loses CO to form the a 1 ion, CH 3 SCH 2 CH 2 CH=NH 2 .
π SIMILAR VOLUMES
The stability of the B,-ion from glycylglycine dipeptides was studied using collision-induced dissociation experiments and ab initi0 calculations. This study reveals that the B,-type ion from glycine should be considered as an electrostatically bound iodmoecule complex, which dissociates into a glyc