Author:
Wang Kai,Gali-Moya Judit,Ruano-Zaragoza Maria,Cain Kathleen,D’Auria Giovanni,Daly Matthew,Barran Perdita,Crevel René,Mills E. N. Clare
Abstract
AbstractSensitisation to the lipid transfer protein Pru p 3 is associated with severe allergic reactions to peach, the proteins stability being thought to play a role in its allergenicity. Lipid binding increases susceptibility of Pru p 3 to digestion and so the impact of bile salts on the in vitro gastrointestinal digestibility of Pru p 3 was investigated and digestion products mapped by SDS-PAGE and mass spectrometry. Bile salts enhanced the digestibility of Pru p 3 resulting in an ensemble of around 100 peptides spanning the protein’s sequence which were linked by disulphide bonds into structures of ~ 5–6 kDa. IgE binding studies with a serum panel from peach allergic subjects showed digestion reduced, but did not abolish, the IgE reactivity of Pru p 3. These data show the importance of including bile salts in vitro digestion systems and emphasise the need to profile of digestion in a manner that allows identification of immunologically relevant disulphide-linked peptide aggregates.
Funder
Chinese Scholarship Council
Biotechnology and Biological Sciences Research Council
Engineering and Physical Sciences Research Council
Publisher
Springer Science and Business Media LLC
Cited by
2 articles.
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