Proteomics and Immunological Analysis of a Novel Shrimp Allergen, Pen m 2

• Published in: The Journal of immunology (1950) Vol. 170; no. 1; pp. 445 - 453
• Main Authors: Yu, Chia-Jung, Lin, Yu-Fen, Chiang, Bor-Luen, Chow, Lu-Ping
• Format: Journal Article
• Language: English
• Published: United States Am Assoc Immnol 01.01.2003
• Subjects: Allergens - analysis; Allergens - blood; Allergens - immunology; Allergens - isolation & purification; Amino Acid Sequence; Animals; Arginine Kinase - analysis; Arginine Kinase - immunology; Arthropod Proteins; Cloning, Molecular; Cross Reactions; Crustacea - enzymology; Crustacea - immunology; Electrophoresis, Gel, Two-Dimensional; Enzyme-Linked Immunosorbent Assay; Humans; Immunoblotting; Immunoglobulin E - biosynthesis; Immunoglobulin E - blood; Molecular Sequence Data; Penaeidae - enzymology; Penaeidae - immunology; Peptide Fragments - analysis; Peptide Fragments - immunology; Proteomics - methods; Rabbits; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.170.1.445

Shellfish are a common cause of adverse food reactions in hypersensitive individuals and shrimp is one of the most frequently reported causes of allergic reactions. A novel allergen from Penaeus monodon, designated Pen m 2, was identified by two-dimensional immunoblotting using sera from subjects with shrimp allergy, followed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry analysis of the peptide digest. This novel allergen was then cloned and the amino acid sequence deduced from the cDNA sequence. The cloned cDNA encoded a 356-aa protein with an acetylated N terminus at Ala2, identified by postsource decay analysis. Comparison of the Pen m 2 sequence with known protein sequences revealed extensive similarity with arginine kinase (EC 2.7.3.3) from crustaceans. Pen m 2 was purified by anion exchange chromatography and shown to have arginine kinase activity and to react with serum IgE from shrimp allergic patients and induce immediate type skin reactions in sensitized patients. Using Pen m 2-specific antisera and polyclonal sera from shrimp-sensitive subjects in a competitive ELISA inhibition assay, Pen m 2 was identified as a novel cross-reactive Crustacea allergen. This novel allergen could be useful in allergy diagnosis and in the treatment of Crustacea-derived allergic disorders.