Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-3
|
pubmed:dateCreated |
1995-8-24
|
pubmed:abstractText |
Peanut allergy is a significant health problem because of the frequency, the potential severity, and the chronicity of the allergic sensitivity. Serum IgE from patients with documented peanut hypersensitivity reactions and a peanut cDNA expression library were used to identify clones that encode peanut allergens. One of the major peanut allergens, Ara h I, was selected from these clones using Ara h I-specific oligonucleotides and polymerase chain reaction technology. The Ara h I clone identified a 2.3-kb mRNA species on a Northern blot containing peanut poly A+RNA. DNA sequence analysis of the cloned inserts revealed that the Ara h I allergen has significant homology with the vicilin seed storage protein family found in most higher plants. The isolation of the Ara h I clones allowed the synthesis of this protein in Escherichia coli cells and subsequent recognition of this recombinant protein in immunoblot analysis using serum IgE from patients with peanut hypersensitivity. With the production of the recombinant peanut protein it will now be possible to address the pathophysiologic and immunologic mechanisms regarding peanut hypersensitivity reactions specifically and food hypersensitivity in general.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Allergens,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Plant,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin E,
http://linkedlifedata.com/resource/pubmed/chemical/Plant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Seed Storage Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/vicilin protein, plant
|
pubmed:status |
MEDLINE
|
pubmed:issn |
1018-2438
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
107
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
248-50
|
pubmed:dateRevised |
2010-11-18
|
pubmed:meshHeading |
pubmed-meshheading:7613142-Allergens,
pubmed-meshheading:7613142-Antibody Specificity,
pubmed-meshheading:7613142-Antigens, Plant,
pubmed-meshheading:7613142-Arachis hypogaea,
pubmed-meshheading:7613142-Base Sequence,
pubmed-meshheading:7613142-DNA, Complementary,
pubmed-meshheading:7613142-Escherichia coli,
pubmed-meshheading:7613142-Food Hypersensitivity,
pubmed-meshheading:7613142-Glycoproteins,
pubmed-meshheading:7613142-Humans,
pubmed-meshheading:7613142-Immunoglobulin E,
pubmed-meshheading:7613142-Molecular Sequence Data,
pubmed-meshheading:7613142-Plant Proteins,
pubmed-meshheading:7613142-Recombinant Fusion Proteins,
pubmed-meshheading:7613142-Seed Storage Proteins,
pubmed-meshheading:7613142-Sequence Homology, Amino Acid
|
pubmed:articleTitle |
Isolation, identification, and characterization of clones encoding antigens responsible for peanut hypersensitivity.
|
pubmed:affiliation |
Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, USA.
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Review
|