Fluorescence correlation spectroscopy assay for gliadin in food (Articolo in rivista)

Type
Label
  • Fluorescence correlation spectroscopy assay for gliadin in food (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1021/ac070475+ (literal)
Alternative label
  • Varriale A.; Rossi M.; Staiano M.; Terpetschnig E.; Barbieri B.; Rossi M.; D'Auria S. (2007)
    Fluorescence correlation spectroscopy assay for gliadin in food
    in Analytical chemistry (Wash.); ACS, American chemical society, Washington, DC (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Varriale A.; Rossi M.; Staiano M.; Terpetschnig E.; Barbieri B.; Rossi M.; D'Auria S. (literal)
Pagina inizio
  • 4687 (literal)
Pagina fine
  • 4689 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 79 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 12 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Institute of Protein Biochemistry, CNR, Naples, Italy, Institute of Food Sciences, CNR, Avellino, Italy, and ISS Inc., Champaign, Illinois 61822 (literal)
Titolo
  • Fluorescence correlation spectroscopy assay for gliadin in food (literal)
Abstract
  • Gliadin proteins are primarily responsible for celiac disease. As gliadin is a complex mixture of proteins difficult to solubilize and to extract from food, it is difficult to develop an assay capable of accurate quantization of gliadin in food for celiac patients. In this work, we present an advanced fluorescence assay for the detection of traces of gliadin in food. The described assay is based on measurement of the fluctuations of fluorescein-labeled gliadin peptides (GP) in a focused laser beam in the absence and in the presence of anti-GP antibodies. A competitive assay based on the utilization of unlabeled GP was developed. The obtained results indicate that the combination of high-avidity IgG antibodies together with the innovative fluorescence immunoassay strategy resulted in a gluten detection limit of 0.006 ppm, which it is much lower than the values reported in the literature. (literal)
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