Literature DB >> 8379214

[Food allergy: identifying and characterizing peanut allergens with patient sera and monoclonal antibodies].

L Uhlemann1, W M Becker, M Schlaak.   

Abstract

The purpose of this study is to improve the diagnosis of peanut allergy. In order to standardize test substances for in vivo and in vitro diagnostic, the type I allergy-associated single components of peanuts have been identified and characterized with the aid of patients' sera and monoclonal antibodies. For allergen detection IEF-immunoprint-, SDS-PAGE-immunoblot- and 2-D electrophoresis-techniques have been used. A comparison of control sera and patients' sera showed that both contained peanut specific IgG-, IgA- and IgM-antibodies. In contrast, peanut-specific IgE-antibodies were only detectable with patients' sera. In IEF-immunoprint the most intensive IgE-bindings showed up in pl-range from pH 5.5 to 7.5. In SDS-PAGE-immunoblot major allergens could be identified at molecular weight ranges of 17, 30, 48 to 66 and 116 kD. Raising monoclonal antibodies against IgE-reactive components from peanut extract resulted in eight antibody-producing hybridoma cell lines, named PN-a to PN-h. ELISA-inhibition tests revealed common epitopes of monoclonal antibodies and patients' antibodies. Moreover, the monoclonal antibodies were tested to see whether they can be used for detection of hidden peanut allergens.

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Year:  1993        PMID: 8379214     DOI: 10.1007/bf01614757

Source DB:  PubMed          Journal:  Z Ernahrungswiss        ISSN: 0044-264X


  24 in total

1.  A review of peanut chemistry. Implications for the standardization of peanut extracts.

Authors:  J W Yunginger; R T Jones
Journal:  Arb Paul Ehrlich Inst Georg Speyer Haus Ferdinand Blum Inst Frankf A M       Date:  1987

2.  Horizontal two-dimensional electrophoresis with immobilized pH gradients using PhastSystem.

Authors:  A Görg; W Postel; S Günther; C Friedrich
Journal:  Electrophoresis       Date:  1988-01       Impact factor: 3.535

3.  Molecular weight determination of membrane protein and glycoprotein subunits by discontinuous gel electrophoresis in dodecyl sulfate.

Authors:  D M Neville; H Glossmann
Journal:  Methods Enzymol       Date:  1974       Impact factor: 1.600

4.  Analysis of allergen components in grass pollen extracts using immunoblotting.

Authors:  H Haas; W M Becker; H J Maasch; M Schlaak
Journal:  Int Arch Allergy Appl Immunol       Date:  1986

5.  Electroblotting of multiple gels: a simple apparatus without buffer tank for rapid transfer of proteins from polyacrylamide to nitrocellulose.

Authors:  J Kyhse-Andersen
Journal:  J Biochem Biophys Methods       Date:  1984-12

6.  Peanut oil is not allergenic to peanut-sensitive individuals.

Authors:  S L Taylor; W W Busse; M I Sachs; J L Parker; J W Yunginger
Journal:  J Allergy Clin Immunol       Date:  1981-11       Impact factor: 10.793

7.  Partial characterization of an allergenic glycoprotein from peanut (Arachis hypogaea L.).

Authors:  D Barnett; M E Howden
Journal:  Biochim Biophys Acta       Date:  1986-06-03

8.  Heterogeneity of grass pollen allergens (Dactylis glomerata) recognized by IgE antibodies in human patients sera by a new nitrocellulose immunoprint technique.

Authors:  G Peltre; J Lapeyre; B David
Journal:  Immunol Lett       Date:  1982-09       Impact factor: 3.685

9.  Immunoassay of peanut allergens in food-processing materials and finished foods.

Authors:  M U Keating; R T Jones; N J Worley; C A Shively; J W Yunginger
Journal:  J Allergy Clin Immunol       Date:  1990-07       Impact factor: 10.793

10.  Peanut protein as a major cause of adverse food reactions in patients with atopic dermatitis.

Authors:  A W Burks; L W Williams; S B Mallory; M A Shirrell; C Williams
Journal:  Allergy Proc       Date:  1989 Jul-Aug
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