Differential Effects of Dry vs. Wet Heating of β-Lactoglobulin on Formation of sRAGE Binding Ligands and sIgE Epitope Recognition

The effect of glycation and aggregation of thermally processed β-lactoglobulin (BLG) on binding to sRAGE and specific immunoglobulin E (sIgE) from cow milk allergic (CMA) patients were investigated. BLG was heated under dry conditions (water activity < 0.7) and wet conditions (in phosphate buffer at pH 7.4) at low temperature (<73 °C) and high temperatures (>90 °C) in the presence or absence of the milk sugar lactose. Nε-(carboxymethyl)-l-lysine (CML) western blot and glycation staining were used to directly identify glycation structures on the protein fractions on SDS-PAGE. Western blot was used to specify sRAGE and sIgE binding fractions. sRAGE binding was highest under wet-heated BLG independent of the presence of the milk sugar lactose. Under wet heating, high-molecular-weight aggregates were most potent and did not require the presence of CML to generate sRAGE binding ligands. In the dry system, sRAGE binding was observed only in the presence of lactose. sIgE binding affinity showed large individual differences and revealed four binding profiles. Dependent on the individual, sIgE binding decreased or increased by wet heating independent of the presence of lactose. Dry heating required the presence of lactose to show increased binding to aggregates in most individuals. This study highlights an important role of heating condition-dependent protein aggregation and glycation in changing the immunogenicity and antigenicity of cow's milk BLG.

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Main Authors: Zenker, Hannah E., Ewaz, Arifa, Deng, Ying, Savelkoul, Huub F.J., van Neerven, R.J., De Jong, Nicolette W., Wichers, Harry J., Hettinga, Kasper A., Teodorowicz, Malgorzata
Format: Article/Letter to editor biblioteca
Language:English
Subjects:CML, IgE binding, aggregation, allergenicity, glycation, sRAGE, β-lactoglobulin,
Online Access:https://research.wur.nl/en/publications/differential-effects-of-dry-vs-wet-heating-of-β-lactoglobulin-on-
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spelling dig-wur-nl-wurpubs-5524702025-01-16 Zenker, Hannah E. Ewaz, Arifa Deng, Ying Savelkoul, Huub F.J. van Neerven, R.J. De Jong, Nicolette W. Wichers, Harry J. Hettinga, Kasper A. Teodorowicz, Malgorzata Article/Letter to editor Nutrients 11 (2019) 6 ISSN: 2072-6643 Differential Effects of Dry vs. Wet Heating of β-Lactoglobulin on Formation of sRAGE Binding Ligands and sIgE Epitope Recognition 2019 The effect of glycation and aggregation of thermally processed β-lactoglobulin (BLG) on binding to sRAGE and specific immunoglobulin E (sIgE) from cow milk allergic (CMA) patients were investigated. BLG was heated under dry conditions (water activity < 0.7) and wet conditions (in phosphate buffer at pH 7.4) at low temperature (<73 °C) and high temperatures (>90 °C) in the presence or absence of the milk sugar lactose. Nε-(carboxymethyl)-l-lysine (CML) western blot and glycation staining were used to directly identify glycation structures on the protein fractions on SDS-PAGE. Western blot was used to specify sRAGE and sIgE binding fractions. sRAGE binding was highest under wet-heated BLG independent of the presence of the milk sugar lactose. Under wet heating, high-molecular-weight aggregates were most potent and did not require the presence of CML to generate sRAGE binding ligands. In the dry system, sRAGE binding was observed only in the presence of lactose. sIgE binding affinity showed large individual differences and revealed four binding profiles. Dependent on the individual, sIgE binding decreased or increased by wet heating independent of the presence of lactose. Dry heating required the presence of lactose to show increased binding to aggregates in most individuals. This study highlights an important role of heating condition-dependent protein aggregation and glycation in changing the immunogenicity and antigenicity of cow's milk BLG. en application/pdf https://research.wur.nl/en/publications/differential-effects-of-dry-vs-wet-heating-of-β-lactoglobulin-on- 10.3390/nu11061432 https://edepot.wur.nl/497141 CML IgE binding aggregation allergenicity glycation sRAGE β-lactoglobulin https://creativecommons.org/licenses/by/4.0/ Wageningen University & Research
institution WUR NL
collection DSpace
country Países bajos
countrycode NL
component Bibliográfico
access En linea
databasecode dig-wur-nl
tag biblioteca
region Europa del Oeste
libraryname WUR Library Netherlands
language English
topic CML
IgE binding
aggregation
allergenicity
glycation
sRAGE
β-lactoglobulin
CML
IgE binding
aggregation
allergenicity
glycation
sRAGE
β-lactoglobulin
spellingShingle CML
IgE binding
aggregation
allergenicity
glycation
sRAGE
β-lactoglobulin
CML
IgE binding
aggregation
allergenicity
glycation
sRAGE
β-lactoglobulin
Zenker, Hannah E.
Ewaz, Arifa
Deng, Ying
Savelkoul, Huub F.J.
van Neerven, R.J.
De Jong, Nicolette W.
Wichers, Harry J.
Hettinga, Kasper A.
Teodorowicz, Malgorzata
Differential Effects of Dry vs. Wet Heating of β-Lactoglobulin on Formation of sRAGE Binding Ligands and sIgE Epitope Recognition
description The effect of glycation and aggregation of thermally processed β-lactoglobulin (BLG) on binding to sRAGE and specific immunoglobulin E (sIgE) from cow milk allergic (CMA) patients were investigated. BLG was heated under dry conditions (water activity < 0.7) and wet conditions (in phosphate buffer at pH 7.4) at low temperature (<73 °C) and high temperatures (>90 °C) in the presence or absence of the milk sugar lactose. Nε-(carboxymethyl)-l-lysine (CML) western blot and glycation staining were used to directly identify glycation structures on the protein fractions on SDS-PAGE. Western blot was used to specify sRAGE and sIgE binding fractions. sRAGE binding was highest under wet-heated BLG independent of the presence of the milk sugar lactose. Under wet heating, high-molecular-weight aggregates were most potent and did not require the presence of CML to generate sRAGE binding ligands. In the dry system, sRAGE binding was observed only in the presence of lactose. sIgE binding affinity showed large individual differences and revealed four binding profiles. Dependent on the individual, sIgE binding decreased or increased by wet heating independent of the presence of lactose. Dry heating required the presence of lactose to show increased binding to aggregates in most individuals. This study highlights an important role of heating condition-dependent protein aggregation and glycation in changing the immunogenicity and antigenicity of cow's milk BLG.
format Article/Letter to editor
topic_facet CML
IgE binding
aggregation
allergenicity
glycation
sRAGE
β-lactoglobulin
author Zenker, Hannah E.
Ewaz, Arifa
Deng, Ying
Savelkoul, Huub F.J.
van Neerven, R.J.
De Jong, Nicolette W.
Wichers, Harry J.
Hettinga, Kasper A.
Teodorowicz, Malgorzata
author_facet Zenker, Hannah E.
Ewaz, Arifa
Deng, Ying
Savelkoul, Huub F.J.
van Neerven, R.J.
De Jong, Nicolette W.
Wichers, Harry J.
Hettinga, Kasper A.
Teodorowicz, Malgorzata
author_sort Zenker, Hannah E.
title Differential Effects of Dry vs. Wet Heating of β-Lactoglobulin on Formation of sRAGE Binding Ligands and sIgE Epitope Recognition
title_short Differential Effects of Dry vs. Wet Heating of β-Lactoglobulin on Formation of sRAGE Binding Ligands and sIgE Epitope Recognition
title_full Differential Effects of Dry vs. Wet Heating of β-Lactoglobulin on Formation of sRAGE Binding Ligands and sIgE Epitope Recognition
title_fullStr Differential Effects of Dry vs. Wet Heating of β-Lactoglobulin on Formation of sRAGE Binding Ligands and sIgE Epitope Recognition
title_full_unstemmed Differential Effects of Dry vs. Wet Heating of β-Lactoglobulin on Formation of sRAGE Binding Ligands and sIgE Epitope Recognition
title_sort differential effects of dry vs. wet heating of β-lactoglobulin on formation of srage binding ligands and sige epitope recognition
url https://research.wur.nl/en/publications/differential-effects-of-dry-vs-wet-heating-of-β-lactoglobulin-on-
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