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Structural basis of the allergenicity to strawberries due to Fra a 1.02
dc.contributor.author | Orozco-Navarrete, Begoña | |
dc.contributor.author | Dupeux, Florine | |
dc.contributor.author | Pott, Delphine | |
dc.contributor.author | Casañal, Ana | |
dc.contributor.author | Garrido-Arandia, María | |
dc.contributor.author | Díaz-Perales, Araceli | |
dc.contributor.author | Merchante-Berg, Catharina | |
dc.contributor.author | Márquez, José A. | |
dc.contributor.author | Valpuesta-Fernández, Victoriano | |
dc.date.accessioned | 2018-07-13T11:47:26Z | |
dc.date.available | 2018-07-13T11:47:26Z | |
dc.date.created | 2018 | |
dc.date.issued | 2018-07-13 | |
dc.identifier.uri | https://hdl.handle.net/10630/16269 | |
dc.description.abstract | Strawberry fruits are highly valued due to their flavor, aroma, and benefits for human health. Despite this, 30% of the population with food hypersensitivity also shows adverse reactions to strawberry (Franz-Oberdorf et al, 2016). The FaFra a 1 protein family, homologs of the major birch pollen allergen Bet v 1, is involved in this allergenicity to strawberry. By RNAseq we have identified transcripts for 18 members of the FaFra a 1 family (from 1.01 to 1.18) in strawberry fruits. Although expressed in all tissues analyzed, each family member presents a unique pattern of expression, which suggests functional specialization for each FaFra a 1 protein. FaFra a 1.02 (Fra2 from now on) is the most expressed one in red fruits and is also the most allergenic among the family members tested (Muñoz et al. 2010; Franz- Oberdorf et al, 2016). In order to understand the molecular bases of this allergenicity we crystalized Fra2 and obtained its structure by X-ray diffraction. Fra2 showed a very high structural homology to Bet v 1, and we asked whether the two proteins were recognized by the immune system in a similar way. For this, we generated five different mutant versions of Fra2 in sites described as important for allergenicity in Bet v 1 (Fernandes et al, 2016), and studied their potential allergenicity as well as their crystal structures. Three of the mutants had substitutions in loop 4 (E46R, D48R, E46/48A) and the other two facing the cavity (A141F and Q64W). Compared to Fra2, all the mutants showed a significant reduction in their capacity to be recognized by the serum of patients with allergies to Bet v 1, and their crystal structures revealed conformational changes in the Bet v 1- IgG interaction sites. Together, these results support that Fra2 and Bet v 1 have similar allergenic determinants We hope this research will aid in understanding how human IgGs interact with Fra2 and might help in the development of new cultivars with a lesser allergenic potential. | en_US |
dc.description.sponsorship | Grants BIO2013-44199R and BES-2014-068723 (MINECO). The authors also acknowledge the support by the Plan Propio from University of Malaga, Campus de Excelencia Internacional de Andalucía. | en_US |
dc.language.iso | eng | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Fresas | en_US |
dc.subject.other | Allergenicity | en_US |
dc.subject.other | Structure | en_US |
dc.subject.other | Strawberry | en_US |
dc.subject.other | Fra | en_US |
dc.title | Structural basis of the allergenicity to strawberries due to Fra a 1.02 | en_US |
dc.type | info:eu-repo/semantics/conferenceObject | en_US |
dc.centro | Facultad de Ciencias | en_US |
dc.relation.eventtitle | XIB Reunión de Biología Molecular de Plantas | en_US |
dc.relation.eventplace | Salamanca, España | en_US |
dc.relation.eventdate | Julio, 2018 | en_US |