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Protease resistance of food proteins: a mixed picture for predicting allergenicity but a useful tool for assessing exposure
- Source :
- Clinical and Translational Allergy, Vol 8, Iss 1, Pp 1-12 (2018), Clinical and translational allergy, 8(1):30. BioMed Central, Akkerdaas, J, Totis, M, Barnett, B, Bell, E, Davis, T, Edrington, T, Glenn, K, Graser, G, Herman, R, Knulst, A, Ladics, G, McClain, S, Poulsen, L K, Ranjan, R, Rascle, J-B, Serrano, H, Speijer, D, Wang, R, Pereira Mouriès, L, Capt, A & van Ree, R 2018, ' Protease resistance of food proteins : a mixed picture for predicting allergenicity but a useful tool for assessing exposure ', Clinical and Translational Allergy, vol. 8, 30 . https://doi.org/10.1186/s13601-018-0216-9, Clinical and Translational Allergy, Clinical and Translational Allergy, 8(1). BioMed Central
- Publication Year :
- 2018
- Publisher :
- Wiley, 2018.
-
Abstract
- Background Susceptibility to pepsin digestion of candidate transgene products is regarded an important parameter in the weight-of-evidence approach for allergenicity risk assessment of genetically modified crops. It has been argued that protocols used for this assessment should better reflect physiological conditions encountered in representative food consumption scenarios. Aim To evaluate whether inclusion of more physiological conditions, such as sub-optimal and lower pepsin concentrations, in combination with pancreatin digestion, improved the performance of digestibility protocols used in characterization of protein stability. Methods Four pairs of established allergens and their related non/weakly-allergenic counterparts (seed albumins, muscle tropomyosins, plant lipid transfer proteins [LTP] and collagens) plus fish parvalbumin, were subjected to nine combinations of pH (1.2–2.5–4.0) and pepsin-to-protein ratio (PPR: 10–1–0.1 U/µg) for pepsin digestion, followed by pancreatin digestion in the presence of bile salts. Digestion was monitored by SDS-PAGE in conjunction with Coomassie staining and immunoblotting using rabbit antisera and human IgE. Results At pH 4.0 and at PPR 0.1 most proteins, both allergen and non-allergen, were highly resistant to pepsin. Under conditions known to favor pepsin proteolysis, the established major allergens Ara h 2, Pru p 3 and Pen a 1 were highly resistant to proteolysis, while the allergen Cyp c 1 was not. However, this resistance to pepsin digestion only made Ara h 2 and to a lesser extent Pen a 1 and Pru p 3 stand out compared to their non-allergenic counterparts. Largely irrespective of preceding pepsin digestion conditions, pancreatin digestion was very effective for all tested proteins, allergens and non-allergens, except for Cyp c 1 and bovine collagen. Conclusions Sub-optimal pH, low pepsin-to protein ratio, and sequential pepsin and pancreatin digestion protocols do not improve the predictive value in distinguish allergens from non-allergens. Digestion conditions facilitating such distinction differ per protein pair. Electronic supplementary material The online version of this article (10.1186/s13601-018-0216-9) contains supplementary material, which is available to authorized users.
- Subjects :
- 0301 basic medicine
Pulmonary and Respiratory Medicine
Proteolysis
medicine.medical_treatment
Immunology
Genetically modified crops
medicine.disease_cause
03 medical and health sciences
0302 clinical medicine
Allergen
Pepsin
medicine
Immunology and Allergy
Antiserum
Protease
medicine.diagnostic_test
biology
business.industry
Research
RC581-607
030104 developmental biology
030228 respiratory system
Biochemistry
biology.protein
Immunologic diseases. Allergy
business
Digestion
Plant lipid transfer proteins
Subjects
Details
- Language :
- English
- ISSN :
- 20457022
- Volume :
- 8
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Clinical and Translational Allergy
- Accession number :
- edsair.doi.dedup.....dad7d5f1eaa2c1704412c2ab02f94235
- Full Text :
- https://doi.org/10.1186/s13601-018-0216-9