International Archives of Allergy and Immunology · 2013 · 46 citations · 23 references
Life SciencesFood ScienceImmunologyAllergyFood ChemistryHypersensitivityFood AllergensFood AllergyIge-mediated AllergyPeanut AllergyProteolytic EnzymesProteolytic ProcessingBasophil Activation TestingBinding CapacityEnzymatic HydrolysisEnzymatic Hydrolysis Of ProteinsFood Oral ImmunotherapyIge-mediated Food AllergyPeanut Allergen ComponentsWestern Blotting
BACKGROUND: Peanut flour is a high-protein, low-oil, powdered material prepared from roasted peanut seed. In addition to being a well-established food ingredient, peanut flour is also the active ingredient in peanut oral immunotherapy trials. Enzymatic hydrolysis was evaluated as a processing strategy to generate hydrolysates from peanut flour with reduced allergenicity. METHODS: Soluble fractions of 10% (w/v) light roasted peanut flour dispersions were hydrolyzed with the following proteases: Alcalase (pH 8.0, 60°C), pepsin (pH 2.0, 37°C) or Flavourzyme (pH 7.0, 50°C) for 60 min. Western blotting, inhibition ELISA and basophil activation tests were used to examine IgE reactivity. RESULTS: Western blotting experiments revealed the hydrolysates retained IgE binding reactivity and these IgE-reactive peptides were primarily Ara h 2 fragments regardless of the protease tested. Inhibition ELISA assays demonstrated that each of the hydrolysates had decreased capacity to bind peanut-specific IgE compared with nonhydrolyzed controls. Basophil activation tests revealed that all hydrolysates were comparable (p > 0.05) to nonhydrolyzed controls in IgE cross-linking capacity. CONCLUSIONS: These results indicate that hydrolysis of peanut flour reduced IgE binding capacity; however, IgE cross-linking capacity during hydrolysis was retained, thus suggesting such hydrolysates are not hypoallergenic.
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Pooja Varshney, Stacie M. Jones, Amy M. Scurlock et al. · Journal of Allergy and Clinical Immunology · 2011 · 560 citations · Full text
Molecular cloning and epitope analysis of the peanut allergen Ara h 3
Pat Rabjohn, Erica M. Helm, J. Steven Stanley et al. · Journal of Clinical Investigation · 1999 · 413 citations · Full text