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413 Effect of Hydrolysis and Polymerization on Bovine Beta-lactoglobulin Immunoreactivity
BACKGROUND: Enzymatic treatments such as hydrolysis with proteases and polymerization using transglutaminase (TG) have been studied to reduce the immunoreactivity of β-Lactoglobulin (β-Lg). Bromelain is a cisteine protease that is not usually used for production of hypoallergenic hydrolysates. TG is...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
World Allergy Organization Journal
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512599/ http://dx.doi.org/10.1097/01.WOX.0000412176.02511.e7 |
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author | Villas-Boas, Mariana Battaglin Sabadin, Isabele Serimarco de Lima Zollner, Ricardo Netto, Flavia Maria |
author_facet | Villas-Boas, Mariana Battaglin Sabadin, Isabele Serimarco de Lima Zollner, Ricardo Netto, Flavia Maria |
author_sort | Villas-Boas, Mariana Battaglin |
collection | PubMed |
description | BACKGROUND: Enzymatic treatments such as hydrolysis with proteases and polymerization using transglutaminase (TG) have been studied to reduce the immunoreactivity of β-Lactoglobulin (β-Lg). Bromelain is a cisteine protease that is not usually used for production of hypoallergenic hydrolysates. TG is an enzyme that catalyses the formation of inter and intramolecular isopeptide bonds between glutamine and lysine residues. The present study is aimed at investigating the antigenic response of β-Lg polymerized by TG pre or post hydrolysis with bromelain. METHODS: β-Lg (donated by Davisco Inc), was hydrolyzed with bromelain (3% protein w/w in distilled water, 25 U enzyme g(−1) of substrate, pH 7.5, 240 min) and then polymerized by TG (7% hydrolysate, 10 or 25 U TG g(−1) protein, 50°C/180 min). When polymerization was carried out pre hydrolysis, β-Lg (7% w/w) was polymerized by TG (10 U TG g(−1) protein, 50°C/180 min) in 0.1 M Cys or after heat treatment (80°C/60 min), and then hydrolyzed under the same conditions previously described. The hydrolysis reaction was monitored by pH-stat method and the samples were evaluated by SDS-PAGE/tricine. Antigenicity was evaluated by Immunoblotting and ELISA assays using sera from mice sensitized with β-Lg (IgE anti-β-Lg). RESULTS: The treatment with TG (10 or 25 U TG g(−1)), post hydrolysis, lead to formation of products with a wide molecular weight (MW) distribution (3 to 26 kDa), and other products with high MW, indicating partial polymerization. The samples obtained from polymerization pre hydrolysis showed bands with low MM (<6.5 kDa) and also products >26 kDa, indicating a partial hydrolysis of the polymers. Immunoblotting analysis showed no reaction towards specific IgE with any of the samples. ELISA assay showed that the IgE-binding response to sample polymerized by TG post or pre hydrolysis with bromelain were significantly reduced (IgE ≤ 35.21 ug mL(−1)) as compared to untreated β-Lg (IgE 216.20 ug mL(−1) ± 27.58) (P < 0.05). CONCLUSIONS: These results suggested that hydrolysis with bromelain combined with polymerization by TG was capable of reducing the antigenicity of β-Lg, being a potential method for modifying the antigenic properties of proteins. |
format | Online Article Text |
id | pubmed-3512599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | World Allergy Organization Journal |
record_format | MEDLINE/PubMed |
spelling | pubmed-35125992012-12-21 413 Effect of Hydrolysis and Polymerization on Bovine Beta-lactoglobulin Immunoreactivity Villas-Boas, Mariana Battaglin Sabadin, Isabele Serimarco de Lima Zollner, Ricardo Netto, Flavia Maria World Allergy Organ J Abstracts of the XXII World Allergy Congress BACKGROUND: Enzymatic treatments such as hydrolysis with proteases and polymerization using transglutaminase (TG) have been studied to reduce the immunoreactivity of β-Lactoglobulin (β-Lg). Bromelain is a cisteine protease that is not usually used for production of hypoallergenic hydrolysates. TG is an enzyme that catalyses the formation of inter and intramolecular isopeptide bonds between glutamine and lysine residues. The present study is aimed at investigating the antigenic response of β-Lg polymerized by TG pre or post hydrolysis with bromelain. METHODS: β-Lg (donated by Davisco Inc), was hydrolyzed with bromelain (3% protein w/w in distilled water, 25 U enzyme g(−1) of substrate, pH 7.5, 240 min) and then polymerized by TG (7% hydrolysate, 10 or 25 U TG g(−1) protein, 50°C/180 min). When polymerization was carried out pre hydrolysis, β-Lg (7% w/w) was polymerized by TG (10 U TG g(−1) protein, 50°C/180 min) in 0.1 M Cys or after heat treatment (80°C/60 min), and then hydrolyzed under the same conditions previously described. The hydrolysis reaction was monitored by pH-stat method and the samples were evaluated by SDS-PAGE/tricine. Antigenicity was evaluated by Immunoblotting and ELISA assays using sera from mice sensitized with β-Lg (IgE anti-β-Lg). RESULTS: The treatment with TG (10 or 25 U TG g(−1)), post hydrolysis, lead to formation of products with a wide molecular weight (MW) distribution (3 to 26 kDa), and other products with high MW, indicating partial polymerization. The samples obtained from polymerization pre hydrolysis showed bands with low MM (<6.5 kDa) and also products >26 kDa, indicating a partial hydrolysis of the polymers. Immunoblotting analysis showed no reaction towards specific IgE with any of the samples. ELISA assay showed that the IgE-binding response to sample polymerized by TG post or pre hydrolysis with bromelain were significantly reduced (IgE ≤ 35.21 ug mL(−1)) as compared to untreated β-Lg (IgE 216.20 ug mL(−1) ± 27.58) (P < 0.05). CONCLUSIONS: These results suggested that hydrolysis with bromelain combined with polymerization by TG was capable of reducing the antigenicity of β-Lg, being a potential method for modifying the antigenic properties of proteins. World Allergy Organization Journal 2012-02-17 /pmc/articles/PMC3512599/ http://dx.doi.org/10.1097/01.WOX.0000412176.02511.e7 Text en Copyright © 2012 by World Allergy Organization |
spellingShingle | Abstracts of the XXII World Allergy Congress Villas-Boas, Mariana Battaglin Sabadin, Isabele Serimarco de Lima Zollner, Ricardo Netto, Flavia Maria 413 Effect of Hydrolysis and Polymerization on Bovine Beta-lactoglobulin Immunoreactivity |
title | 413 Effect of Hydrolysis and Polymerization on Bovine Beta-lactoglobulin Immunoreactivity |
title_full | 413 Effect of Hydrolysis and Polymerization on Bovine Beta-lactoglobulin Immunoreactivity |
title_fullStr | 413 Effect of Hydrolysis and Polymerization on Bovine Beta-lactoglobulin Immunoreactivity |
title_full_unstemmed | 413 Effect of Hydrolysis and Polymerization on Bovine Beta-lactoglobulin Immunoreactivity |
title_short | 413 Effect of Hydrolysis and Polymerization on Bovine Beta-lactoglobulin Immunoreactivity |
title_sort | 413 effect of hydrolysis and polymerization on bovine beta-lactoglobulin immunoreactivity |
topic | Abstracts of the XXII World Allergy Congress |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512599/ http://dx.doi.org/10.1097/01.WOX.0000412176.02511.e7 |
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