Protease recognition sites in Bet v 1a are cryptic, explaining its slow processing relevant to its allergenicity

Sci Rep. 2015 Aug 3:5:12707. doi: 10.1038/srep12707.

Abstract

Despite a high similarity with homologous protein families, only few proteins trigger an allergic immune response with characteristic TH2 polarization. This puzzling observation is illustrated by the major birch pollen allergen Bet v 1a and its hypoallergenic protein isoforms, e.g., Bet v 1d. Given the key role of proteolytic processing in antigen presentation and T cell polarization, we investigated the recognition of Bet v 1 isoforms by the relevant protease cathepsin S. We found that at moderately acidic pH values Bet v 1a bound to cathepsin S with significantly lower affinity and was more slowly cleaved than its hypoallergenic isoform Bet v 1d. Only at pH values ≤ 4.5 the known proteolytic cleavage sites in Bet v 1a became accessible, resulting in a strong increase in affinity towards cathepsin S. Antigen processing and class II MHC loading occurs at moderately acidic compartments where processing of Bet v 1a and Bet v 1d differs distinctly. This difference translates into low and high density class II MHC loading and subsequently in TH2 and TH1 polarization, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allergens / chemistry
  • Allergens / immunology
  • Allergens / metabolism*
  • Amino Acid Sequence
  • Antigens, Plant / chemistry
  • Antigens, Plant / immunology
  • Antigens, Plant / metabolism*
  • Betula / immunology
  • Binding Sites
  • Cathepsins / metabolism*
  • Humans
  • Molecular Sequence Data
  • Plant Proteins / chemistry
  • Plant Proteins / immunology
  • Plant Proteins / metabolism
  • Pollen / immunology
  • Sequence Alignment

Substances

  • Allergens
  • Antigens, Plant
  • Plant Proteins
  • Bet v 1 allergen, Betula
  • Cathepsins
  • cathepsin S