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In silico epitope prediction, expression and functional analysis of Per a 10 allergen from the American cockroach

Cockroach (CR) allergies caused by the American cockroach hyave been recognized to be repsonsible for IgE-mediated type I hypersensitivity worldwide. Per a 10 is one of the recognized main allergens of the American CR. In a previous study, we examined another American CR allergen, Per a 9 in patient...

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Autores principales: Tong, Xunliang, Guo, Miao, Jin, Min, Chen, Hao, Li, Yanming, Wei, Ji-Fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117736/
https://www.ncbi.nlm.nih.gov/pubmed/27840898
http://dx.doi.org/10.3892/ijmm.2016.2790
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author Tong, Xunliang
Guo, Miao
Jin, Min
Chen, Hao
Li, Yanming
Wei, Ji-Fu
author_facet Tong, Xunliang
Guo, Miao
Jin, Min
Chen, Hao
Li, Yanming
Wei, Ji-Fu
author_sort Tong, Xunliang
collection PubMed
description Cockroach (CR) allergies caused by the American cockroach hyave been recognized to be repsonsible for IgE-mediated type I hypersensitivity worldwide. Per a 10 is one of the recognized main allergens of the American CR. In a previous study, we examined another American CR allergen, Per a 9 in patients with CR allergies and examined epitope sequences in this allergen. In the present study, we aimed to examine epitope sequences in the Per a 10 allergen. for this purpose, the Per a 10 gene was cloned and expressed in Escherichia coli (E. coli) systems. Our results revealed that 9 out of 16 (56.3%) sera from patients with American CR allergies reacted to Per a10, as assessed by ELISA, confirming that Per a 10 is a major allergen of the American CR. Our results also revealed that the expression of CD63 and CCR3 on passively sensitized basophils (obtained sera of patients with American CR allergies) was increased by approximately 2.3-fold, indicating that recombinant Per a 10 is functionally active. In addition, 3 immunoinformatics tools, namely the DNAStar Protean system, the Bioinformatics Predicted Antigenic Peptides (BPAP) system and the BepiPred 1.0 server were used to predict the peptides and the results revealed 8 peptides (2–12, 55–67, 98–120, 125–133, 149–160, 170–182, 201–208 and 223–227) as potential B cell epitopes of the Per a 10 allergen. Moreover, Per a 10 was predicted to have 3 T cell epitope sequences, namely 83–92, 139–147 and 162–170. The findings of our study on the CR allergen may prove to be useful in the development of peptide-based vaccine for the prevention and/or treatment of CR allergies.
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spelling pubmed-51177362016-11-28 In silico epitope prediction, expression and functional analysis of Per a 10 allergen from the American cockroach Tong, Xunliang Guo, Miao Jin, Min Chen, Hao Li, Yanming Wei, Ji-Fu Int J Mol Med Articles Cockroach (CR) allergies caused by the American cockroach hyave been recognized to be repsonsible for IgE-mediated type I hypersensitivity worldwide. Per a 10 is one of the recognized main allergens of the American CR. In a previous study, we examined another American CR allergen, Per a 9 in patients with CR allergies and examined epitope sequences in this allergen. In the present study, we aimed to examine epitope sequences in the Per a 10 allergen. for this purpose, the Per a 10 gene was cloned and expressed in Escherichia coli (E. coli) systems. Our results revealed that 9 out of 16 (56.3%) sera from patients with American CR allergies reacted to Per a10, as assessed by ELISA, confirming that Per a 10 is a major allergen of the American CR. Our results also revealed that the expression of CD63 and CCR3 on passively sensitized basophils (obtained sera of patients with American CR allergies) was increased by approximately 2.3-fold, indicating that recombinant Per a 10 is functionally active. In addition, 3 immunoinformatics tools, namely the DNAStar Protean system, the Bioinformatics Predicted Antigenic Peptides (BPAP) system and the BepiPred 1.0 server were used to predict the peptides and the results revealed 8 peptides (2–12, 55–67, 98–120, 125–133, 149–160, 170–182, 201–208 and 223–227) as potential B cell epitopes of the Per a 10 allergen. Moreover, Per a 10 was predicted to have 3 T cell epitope sequences, namely 83–92, 139–147 and 162–170. The findings of our study on the CR allergen may prove to be useful in the development of peptide-based vaccine for the prevention and/or treatment of CR allergies. D.A. Spandidos 2016-12 2016-10-26 /pmc/articles/PMC5117736/ /pubmed/27840898 http://dx.doi.org/10.3892/ijmm.2016.2790 Text en Copyright: © Tong et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Tong, Xunliang
Guo, Miao
Jin, Min
Chen, Hao
Li, Yanming
Wei, Ji-Fu
In silico epitope prediction, expression and functional analysis of Per a 10 allergen from the American cockroach
title In silico epitope prediction, expression and functional analysis of Per a 10 allergen from the American cockroach
title_full In silico epitope prediction, expression and functional analysis of Per a 10 allergen from the American cockroach
title_fullStr In silico epitope prediction, expression and functional analysis of Per a 10 allergen from the American cockroach
title_full_unstemmed In silico epitope prediction, expression and functional analysis of Per a 10 allergen from the American cockroach
title_short In silico epitope prediction, expression and functional analysis of Per a 10 allergen from the American cockroach
title_sort in silico epitope prediction, expression and functional analysis of per a 10 allergen from the american cockroach
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117736/
https://www.ncbi.nlm.nih.gov/pubmed/27840898
http://dx.doi.org/10.3892/ijmm.2016.2790
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