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Protease resistance of food proteins: a mixed picture for predicting allergenicity but a useful tool for assessing exposure
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 physi...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085708/ https://www.ncbi.nlm.nih.gov/pubmed/30116520 http://dx.doi.org/10.1186/s13601-018-0216-9 |
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author | Akkerdaas, Jaap Totis, Muriel Barnett, Brian Bell, Erin Davis, Tom Edrington, Thomas Glenn, Kevin Graser, Gerson Herman, Rod Knulst, Andre Ladics, Gregory McClain, Scott Poulsen, Lars K. Ranjan, Rakesh Rascle, Jean-Baptiste Serrano, Hector Speijer, Dave Wang, Rong Pereira Mouriès, Lucilia Capt, Annabelle van Ree, Ronald |
author_facet | Akkerdaas, Jaap Totis, Muriel Barnett, Brian Bell, Erin Davis, Tom Edrington, Thomas Glenn, Kevin Graser, Gerson Herman, Rod Knulst, Andre Ladics, Gregory McClain, Scott Poulsen, Lars K. Ranjan, Rakesh Rascle, Jean-Baptiste Serrano, Hector Speijer, Dave Wang, Rong Pereira Mouriès, Lucilia Capt, Annabelle van Ree, Ronald |
author_sort | Akkerdaas, Jaap |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6085708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60857082018-08-16 Protease resistance of food proteins: a mixed picture for predicting allergenicity but a useful tool for assessing exposure Akkerdaas, Jaap Totis, Muriel Barnett, Brian Bell, Erin Davis, Tom Edrington, Thomas Glenn, Kevin Graser, Gerson Herman, Rod Knulst, Andre Ladics, Gregory McClain, Scott Poulsen, Lars K. Ranjan, Rakesh Rascle, Jean-Baptiste Serrano, Hector Speijer, Dave Wang, Rong Pereira Mouriès, Lucilia Capt, Annabelle van Ree, Ronald Clin Transl Allergy Research 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. BioMed Central 2018-08-10 /pmc/articles/PMC6085708/ /pubmed/30116520 http://dx.doi.org/10.1186/s13601-018-0216-9 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Akkerdaas, Jaap Totis, Muriel Barnett, Brian Bell, Erin Davis, Tom Edrington, Thomas Glenn, Kevin Graser, Gerson Herman, Rod Knulst, Andre Ladics, Gregory McClain, Scott Poulsen, Lars K. Ranjan, Rakesh Rascle, Jean-Baptiste Serrano, Hector Speijer, Dave Wang, Rong Pereira Mouriès, Lucilia Capt, Annabelle van Ree, Ronald Protease resistance of food proteins: a mixed picture for predicting allergenicity but a useful tool for assessing exposure |
title | Protease resistance of food proteins: a mixed picture for predicting allergenicity but a useful tool for assessing exposure |
title_full | Protease resistance of food proteins: a mixed picture for predicting allergenicity but a useful tool for assessing exposure |
title_fullStr | Protease resistance of food proteins: a mixed picture for predicting allergenicity but a useful tool for assessing exposure |
title_full_unstemmed | Protease resistance of food proteins: a mixed picture for predicting allergenicity but a useful tool for assessing exposure |
title_short | Protease resistance of food proteins: a mixed picture for predicting allergenicity but a useful tool for assessing exposure |
title_sort | protease resistance of food proteins: a mixed picture for predicting allergenicity but a useful tool for assessing exposure |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085708/ https://www.ncbi.nlm.nih.gov/pubmed/30116520 http://dx.doi.org/10.1186/s13601-018-0216-9 |
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