Cloning of the minor allergen Api g 4 profilin from celery (Apium graveolens) and its cross-reactivity with birch pollen profilin Bet v 2

Clin Exp Allergy. 2000 Jul;30(7):962-71. doi: 10.1046/j.1365-2222.2000.00821.x.

Abstract

Background: Profilin is a panallergen that is recognized by IgE from about 20% of birch pollen- and plant food-allergic patients. A subgroup of celery-allergic patients shows IgE-reactivity with this minor allergen. To investigate the IgE-binding potential and cross-reactivity of celery profilin at the molecular level, this study was aimed at the cloning and immunological characterization of this allergen.

Objectives: Cloning, expression and purification of profilin from celery tuber to characterize its immunological properties and its cross-reactivity with birch pollen profilin.

Methods: Cloning of celery profilin was performed by polymerase chain reaction using degenerated primers and a 5'RACE method for the identification of the unknown 5'-end of the cDNA. Expression was carried out in Escherichia coli BL21 (DE3) using a modified vector pET-30a. The recombinant profilin was purified by affinity chromatography on poly L-proline coupled to sepharose. Immunological characterization was performed by immunoblotting, EAST and IgE-inhibition experiments.

Results: The coding region of the cDNA of celery profilin was identified as a 399-bp open reading frame, coding for a protein of 133 amino acids with a calculated molecular weight of 14.3 kDa. The deduced amino acid sequence of the corresponding protein showed high identity with other plant profilins (71-82%) recently described as allergens. Celery profilin was isolated as highly pure nonfusion protein. The IgE-reactivity of celery profilin was similar to that of natural protein. Seven of 17 celery-allergic patients tested presented specific IgE-antibodies to the recombinant protein tested by immunoblotting. Inhibition experiments showed high cross-reactivity of IgE with both profilins from celery and birch pollen. Moreover, the biological activity of recombinant celery profilin was demonstrated by a histamine release assay.

Conclusions: Celery profilin is an important allergenic compound in celery and shows high homology to birch pollen profilin, Bet v 2. According to the revised IUIS allergen nomenclature, we suggest naming the celery profilin Api g 4. In addition to the cross-reacting major allergens Api g 1 and Bet v 1, birch pollinosis and associated allergies to celery can therefore additionally be explained by the cross-reactivity between homologous profilins. Moreover, recombinant Api g 4 may be used for target-specific diagnosis and structural analyses.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Allergens* / genetics
  • Allergens* / immunology
  • Allergens* / isolation & purification
  • Amino Acid Sequence
  • Apiaceae / adverse effects
  • Apiaceae / chemistry
  • Apiaceae / immunology*
  • Base Sequence
  • Cloning, Molecular
  • Contractile Proteins*
  • Cross Reactions / immunology
  • DNA Primers / chemistry
  • Double-Blind Method
  • Electrophoresis, Polyacrylamide Gel
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Food Hypersensitivity / etiology
  • Food Hypersensitivity / immunology
  • Gene Expression
  • Histamine Release
  • Humans
  • Microfilament Proteins* / genetics
  • Microfilament Proteins* / immunology
  • Microfilament Proteins* / isolation & purification
  • Molecular Sequence Data
  • Plant Proteins* / genetics
  • Plant Proteins* / immunology
  • Plant Proteins* / isolation & purification
  • Pollen / adverse effects
  • Pollen / chemistry
  • Pollen / immunology*
  • Polymerase Chain Reaction
  • Profilins
  • RNA / isolation & purification
  • Recombinant Proteins / genetics
  • Recombinant Proteins / immunology
  • Sequence Analysis, DNA

Substances

  • Allergens
  • Contractile Proteins
  • DNA Primers
  • Microfilament Proteins
  • Plant Proteins
  • Profilins
  • Recombinant Proteins
  • RNA