Articles producció científica> Enginyeria Química

DNA aptamers against the lup an 1 food allergen

  • Datos identificativos

    Identificador: PC:137
    Handle: http://hdl.handle.net/20.500.11797/PC137
  • Autores:

    Nadal, P.
    Pinto, A.
    Svobodova, M.
    Canela, N.
    O'Sullivan, C.K.
  • Otros:

    Autor según el artículo: Nadal, P. Pinto, A. Svobodova, M. Canela, N. O'Sullivan, C.K.
    Versión del articulo depositado: info:eu-repo/semantics/publishedVersion
    Enlace a la fuente original: http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0035253
    Departamento: Enginyeria Química
    Autor/es de la URV: Nadal, P., Pinto, A., Svobodova, M., Canela, N., O'Sullivan, C.K.
    DOI del artículo: 10.1371/journal.pone.0035253
    Resumen: Using in vitro selection, high affinity DNA aptamers to the food allergen Lup an 1, ß-conglutin, were selected from a pool of DNA, 93 bases in length, containing a randomised sequence of 49 bases. ß-conglutin was purified from lupin flour and chemically crosslinked to carboxylated magnetic beads. Peptide mass fingerprinting was used to confirm the presence of the ß-conglutin. Single stranded DNA was generated from the randomised pool using T7 Gene 6 Exonuclease and was subsequently incubated with the magnetic beads and the captured DNA was released and amplified prior to a further round of Systematic Evolution of Ligands by Exponential Enrichment (SELEX). Evolution was monitored using enzyme linked oligonucleotide assay and surface plasmon resonance. Once a plateau in evolution was reached, the isolated DNA sequences were cloned and sequenced. The consensus motif was identified via alignment of the sequences and the affinities of these sequences for immobilised ß-conglutin were determined using surface plasmon resonance. The selected aptamer was demonstrated to be highly specific, showing no cross-reactivity with other flour ingredients or with other conglutin fractions of lupin. The secondary structures of the selected aptamers were predicted using m-fold. Finally, the functionality of the selected aptamers was demonstrated using a competitive assay for the quantitative detection of ß-conglutin. Future work will focus on structure elucidation and truncation of the selected sequences to generate a smaller aptamer for application to the analysis of the Lup an 1 allergen in foodstuffs
    Entidad: Universitat Rovira i Virgili.
    Año de publicación de la revista: 2012
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 1932-6203
    Volumen de revista: 7
  • Palabras clave:

    Aptamers, Nucleotide
    1932-6203
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