Characterization of mutants of a highly cross-reactive calcium-binding protein from Brassica pollen for allergen-specific immunotherapy

Tetiana Garmatiuk, Ines Swoboda, Anna Twardosz-Kropfmüller, Fabio Dall'Antonia, Walter Keller, Mohan B. Singh, Prem L. Bhalla, Takashi Okada, Kinya Toriyama, Milena Weber, Minoo Ghannadan, Wolfgang R. Sperr, Katharina Blatt, Peter Valent, Brigitte Klein, Verena Niederberger, Mirela Curin, Nadja Balic, Susanne Spitzauer, Rudolf Valenta

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)

Abstract

The major turnip (Brassica rapa) pollen allergen, belongs to a family of calcium-binding proteins (i.e., two EF-hand proteins), which occur as highly cross-reactive allergens in pollen of weeds, grasses and trees. In this study, the IgE binding capacity and allergenic activity of three recombinant allergen variants containing mutations in their calcium-binding sites were analyzed in sensitized patients with the aim to identify the most suitable hypoallergenic molecule for specific immunotherapy.Analysis of the wildtype allergen and the mutants regarding IgE reactivity and activation of basophils in allergic patients indicated that the allergen derivative mutated in both calcium-binding domains had the lowest allergenic activity. Gel filtration and circular dichroism experiments showed that both, the wildtype and the double mutant, occurred as dimers in solution and assumed alpha-helical fold, respectively. However, both fold and thermal stability were considerably reduced in the double mutant. The use of bioinformatic tools for evaluation of the solvent accessibility and charge distribution suggested that the reduced IgE reactivity and different structural properties of the double mutant may be due to a loss of negatively charged amino acids on the surface. Interestingly, immunization of rabbits showed that only the double mutant but not the wildtype allergen induced IgG antibodies which recognized the allergen and blocked binding of allergic patients IgE.Due to the extensive structural similarity and cross-reactivity between calcium-binding pollen allergens the hypoallergenic double mutant may be useful not only for immunotherapy of turnip pollen allergy, but also for the treatment of allergies to other two EF-hand pollen allergens.

Original languageEnglish
Pages (from-to)1155-1165
Number of pages11
JournalImmunobiology
Volume218
Issue number9
DOIs
Publication statusPublished - 2013 Sep 1

Keywords

  • Allergen
  • Allergy
  • Brassica
  • Calcium-binding allergen
  • Cross-reactivity
  • Hypoallergenic mutants
  • Immunotherapy

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology
  • Hematology

Fingerprint Dive into the research topics of 'Characterization of mutants of a highly cross-reactive calcium-binding protein from Brassica pollen for allergen-specific immunotherapy'. Together they form a unique fingerprint.

Cite this