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Intra‐species cross‐reactivity of house dust mite allergens separated by protein blotting and detected by selective elution of mite components and IgE antibodies
Author(s) -
O'Neill Geraldine M.,
Baldo Brian A.
Publication year - 1993
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/elps.11501401147
Subject(s) - blot , allergen , chemistry , nitrocellulose , antibody , mite , gel electrophoresis , house dust mite , immunoglobulin e , sodium dodecyl sulfate , polyacrylamide gel electrophoresis , antigen , chromatography , allergy , microbiology and biotechnology , biochemistry , immunology , biology , enzyme , botany , membrane , gene
A complex and varied antibody response to allergens, in particular Dermatophagoides pteronyssinus , is observed in the serum of allergic patients. To examine the role of cross‐reacting antigenic determinants in allergy, a strategy has been devised for isolating antibody populations that bind to individual polypeptides of an allergen source separated by sodium dodecyl sulfate‐polyacrylamide electrophoresis and electroblotted to nitrocellulose. Polypeptides are identified on the blots, desorbed and coupled to CNBr‐activated paper discs. The coupled discs are then used as immunoadsorbent surfaces for the binding of antibodies from allergic sera. Antibodies eluted from the polypeptide immunoadsorbents are then used to reprobe protein blots of the allergen. Results are presented which demonstrate strong cross‐reaction between two major mite allergens, Der p I and Der p III, and some weaker intra‐species cross‐reactivities.