Identification of cross-reactive B-cell epitopes between Bos d 9.0101(<i>Bos Taurus</i>) and Gly m 5.0101 (<i>Glycine max</i>) by epitope mapping MALDI-TOF MS
- Autores
- Candreva, Ángela María; Ferrer Navarro, Mario; Bronsoms, Silvia; Quiroga, Alejandra Viviana; Curciarello, Renata; Cauerhff, Ana Albina; Petruccelli, Silvana; Docena, Guillermo Horacio; Trejo, Sebastián Alejandro
- Año de publicación
- 2017
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Exposure to cow’smilk constitutes one of the most common causes of food allergy. In addition, exposure to soy proteins has become relevant in a restricted proportion ofmilk allergic pediatric patients treated with soy formulae as a dairy substitute, because of the cross-allergenicity described between soy and milk proteins. We have previously identified several cross-reactive allergens between milk and soy that may explain this intolerance. The purpose of the present work was to identify epitopes in the purified αS1-casein and the recombinant soy allergen Gly m 5.0101 (Gly m 5) using an α-casein-specific monoclonal antibody (1D5 mAb) through two different approaches for epitope mapping, to understand cross-reactivity between milk and soy. The 1D5 mAb was immobilized onto magnetic beads, incubated with the peptide mixture previously obtained by enzymatic digestion of the allergens, and the captured peptides were identified by MALDI-TOFMS analysis. On a second approach, the peptidemixture was resolved by RP-HPLC and immunodominant peptides were identified by dot blot with the mAb. Finally, recognized peptides were sequenced by MALDI-TOF MS. This novel MS based approach led us to identify and characterize four peptides on α-casein and three peptides on Gly m 5 with a common core motif. Information obtained from these cross-reactive epitopes allows us to gain valuable insight into the molecular mechanisms of cross-reactivity, to further develop new and more effective vaccines for food allergy.
Facultad de Ciencias Exactas
Instituto de Estudios Inmunológicos y Fisiopatológicos
Instituto Multidisciplinario de Biología Celular - Materia
-
Ciencias Exactas
Biología
Bos d 9.0101
cow’s milk
cross-reactivity
epitope mapping
Gly m 5.0101
MALDI-TOF MS
soybean - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/107570
Ver los metadatos del registro completo
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Identification of cross-reactive B-cell epitopes between Bos d 9.0101(<i>Bos Taurus</i>) and Gly m 5.0101 (<i>Glycine max</i>) by epitope mapping MALDI-TOF MSCandreva, Ángela MaríaFerrer Navarro, MarioBronsoms, SilviaQuiroga, Alejandra VivianaCurciarello, RenataCauerhff, Ana AlbinaPetruccelli, SilvanaDocena, Guillermo HoracioTrejo, Sebastián AlejandroCiencias ExactasBiologíaBos d 9.0101cow’s milkcross-reactivityepitope mappingGly m 5.0101MALDI-TOF MSsoybeanExposure to cow’smilk constitutes one of the most common causes of food allergy. In addition, exposure to soy proteins has become relevant in a restricted proportion ofmilk allergic pediatric patients treated with soy formulae as a dairy substitute, because of the cross-allergenicity described between soy and milk proteins. We have previously identified several cross-reactive allergens between milk and soy that may explain this intolerance. The purpose of the present work was to identify epitopes in the purified αS1-casein and the recombinant soy allergen Gly m 5.0101 (Gly m 5) using an α-casein-specific monoclonal antibody (1D5 mAb) through two different approaches for epitope mapping, to understand cross-reactivity between milk and soy. The 1D5 mAb was immobilized onto magnetic beads, incubated with the peptide mixture previously obtained by enzymatic digestion of the allergens, and the captured peptides were identified by MALDI-TOFMS analysis. On a second approach, the peptidemixture was resolved by RP-HPLC and immunodominant peptides were identified by dot blot with the mAb. Finally, recognized peptides were sequenced by MALDI-TOF MS. This novel MS based approach led us to identify and characterize four peptides on α-casein and three peptides on Gly m 5 with a common core motif. Information obtained from these cross-reactive epitopes allows us to gain valuable insight into the molecular mechanisms of cross-reactivity, to further develop new and more effective vaccines for food allergy.Facultad de Ciencias ExactasInstituto de Estudios Inmunológicos y FisiopatológicosInstituto Multidisciplinario de Biología Celular2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/107570enginfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/pmic.201700069info:eu-repo/semantics/altIdentifier/issn/1615-9861info:eu-repo/semantics/altIdentifier/doi/10.1002/pmic.201700069info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-03T10:56:17Zoai:sedici.unlp.edu.ar:10915/107570Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-03 10:56:17.69SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Identification of cross-reactive B-cell epitopes between Bos d 9.0101(<i>Bos Taurus</i>) and Gly m 5.0101 (<i>Glycine max</i>) by epitope mapping MALDI-TOF MS |
title |
Identification of cross-reactive B-cell epitopes between Bos d 9.0101(<i>Bos Taurus</i>) and Gly m 5.0101 (<i>Glycine max</i>) by epitope mapping MALDI-TOF MS |
spellingShingle |
Identification of cross-reactive B-cell epitopes between Bos d 9.0101(<i>Bos Taurus</i>) and Gly m 5.0101 (<i>Glycine max</i>) by epitope mapping MALDI-TOF MS Candreva, Ángela María Ciencias Exactas Biología Bos d 9.0101 cow’s milk cross-reactivity epitope mapping Gly m 5.0101 MALDI-TOF MS soybean |
title_short |
Identification of cross-reactive B-cell epitopes between Bos d 9.0101(<i>Bos Taurus</i>) and Gly m 5.0101 (<i>Glycine max</i>) by epitope mapping MALDI-TOF MS |
title_full |
Identification of cross-reactive B-cell epitopes between Bos d 9.0101(<i>Bos Taurus</i>) and Gly m 5.0101 (<i>Glycine max</i>) by epitope mapping MALDI-TOF MS |
title_fullStr |
Identification of cross-reactive B-cell epitopes between Bos d 9.0101(<i>Bos Taurus</i>) and Gly m 5.0101 (<i>Glycine max</i>) by epitope mapping MALDI-TOF MS |
title_full_unstemmed |
Identification of cross-reactive B-cell epitopes between Bos d 9.0101(<i>Bos Taurus</i>) and Gly m 5.0101 (<i>Glycine max</i>) by epitope mapping MALDI-TOF MS |
title_sort |
Identification of cross-reactive B-cell epitopes between Bos d 9.0101(<i>Bos Taurus</i>) and Gly m 5.0101 (<i>Glycine max</i>) by epitope mapping MALDI-TOF MS |
dc.creator.none.fl_str_mv |
Candreva, Ángela María Ferrer Navarro, Mario Bronsoms, Silvia Quiroga, Alejandra Viviana Curciarello, Renata Cauerhff, Ana Albina Petruccelli, Silvana Docena, Guillermo Horacio Trejo, Sebastián Alejandro |
author |
Candreva, Ángela María |
author_facet |
Candreva, Ángela María Ferrer Navarro, Mario Bronsoms, Silvia Quiroga, Alejandra Viviana Curciarello, Renata Cauerhff, Ana Albina Petruccelli, Silvana Docena, Guillermo Horacio Trejo, Sebastián Alejandro |
author_role |
author |
author2 |
Ferrer Navarro, Mario Bronsoms, Silvia Quiroga, Alejandra Viviana Curciarello, Renata Cauerhff, Ana Albina Petruccelli, Silvana Docena, Guillermo Horacio Trejo, Sebastián Alejandro |
author2_role |
author author author author author author author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Biología Bos d 9.0101 cow’s milk cross-reactivity epitope mapping Gly m 5.0101 MALDI-TOF MS soybean |
topic |
Ciencias Exactas Biología Bos d 9.0101 cow’s milk cross-reactivity epitope mapping Gly m 5.0101 MALDI-TOF MS soybean |
dc.description.none.fl_txt_mv |
Exposure to cow’smilk constitutes one of the most common causes of food allergy. In addition, exposure to soy proteins has become relevant in a restricted proportion ofmilk allergic pediatric patients treated with soy formulae as a dairy substitute, because of the cross-allergenicity described between soy and milk proteins. We have previously identified several cross-reactive allergens between milk and soy that may explain this intolerance. The purpose of the present work was to identify epitopes in the purified αS1-casein and the recombinant soy allergen Gly m 5.0101 (Gly m 5) using an α-casein-specific monoclonal antibody (1D5 mAb) through two different approaches for epitope mapping, to understand cross-reactivity between milk and soy. The 1D5 mAb was immobilized onto magnetic beads, incubated with the peptide mixture previously obtained by enzymatic digestion of the allergens, and the captured peptides were identified by MALDI-TOFMS analysis. On a second approach, the peptidemixture was resolved by RP-HPLC and immunodominant peptides were identified by dot blot with the mAb. Finally, recognized peptides were sequenced by MALDI-TOF MS. This novel MS based approach led us to identify and characterize four peptides on α-casein and three peptides on Gly m 5 with a common core motif. Information obtained from these cross-reactive epitopes allows us to gain valuable insight into the molecular mechanisms of cross-reactivity, to further develop new and more effective vaccines for food allergy. Facultad de Ciencias Exactas Instituto de Estudios Inmunológicos y Fisiopatológicos Instituto Multidisciplinario de Biología Celular |
description |
Exposure to cow’smilk constitutes one of the most common causes of food allergy. In addition, exposure to soy proteins has become relevant in a restricted proportion ofmilk allergic pediatric patients treated with soy formulae as a dairy substitute, because of the cross-allergenicity described between soy and milk proteins. We have previously identified several cross-reactive allergens between milk and soy that may explain this intolerance. The purpose of the present work was to identify epitopes in the purified αS1-casein and the recombinant soy allergen Gly m 5.0101 (Gly m 5) using an α-casein-specific monoclonal antibody (1D5 mAb) through two different approaches for epitope mapping, to understand cross-reactivity between milk and soy. The 1D5 mAb was immobilized onto magnetic beads, incubated with the peptide mixture previously obtained by enzymatic digestion of the allergens, and the captured peptides were identified by MALDI-TOFMS analysis. On a second approach, the peptidemixture was resolved by RP-HPLC and immunodominant peptides were identified by dot blot with the mAb. Finally, recognized peptides were sequenced by MALDI-TOF MS. This novel MS based approach led us to identify and characterize four peptides on α-casein and three peptides on Gly m 5 with a common core motif. Information obtained from these cross-reactive epitopes allows us to gain valuable insight into the molecular mechanisms of cross-reactivity, to further develop new and more effective vaccines for food allergy. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://sedici.unlp.edu.ar/handle/10915/107570 |
url |
http://sedici.unlp.edu.ar/handle/10915/107570 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/pmic.201700069 info:eu-repo/semantics/altIdentifier/issn/1615-9861 info:eu-repo/semantics/altIdentifier/doi/10.1002/pmic.201700069 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
dc.format.none.fl_str_mv |
application/pdf |
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