Structure of the Major Apple Allergen Mal d 1

J Agric Food Chem. 2017 Mar 1;65(8):1606-1612. doi: 10.1021/acs.jafc.6b05752. Epub 2017 Feb 15.

Abstract

More than 70% of birch pollen-allergic patients develop allergic cross-reactions to the major allergen found in apple fruits (Malus domestica), the 17.5 kDa protein Mal d 1. Allergic reactions against this protein result from initial sensitization to the major allergen from birch pollen, Bet v 1. Immunologic cross-reactivity of Bet v 1-specific IgE antibodies with Mal d 1 after apple consumption can subsequently provoke severe oral allergic syndromes. This study presents the three-dimensional NMR solution structure of Mal d 1 (isoform Mal d 1.0101, initially cloned from 'Granny Smith' apples). This protein is composed of a seven-stranded antiparallel β-sheet and three α-helices that form a large internal cavity, similar to Bet v 1 and other cross-reactive food allergens. The Mal d 1 structure provides the basis for elucidating the details of allergic cross-reactivity between birch pollen and apple allergens on a molecular level.

Keywords: Mal d 1; Malus domestica; allergen; structure.

MeSH terms

  • Antigens, Plant / chemistry*
  • Antigens, Plant / immunology
  • Malus / chemistry*
  • Malus / immunology
  • Models, Molecular
  • Plant Proteins / chemistry*
  • Plant Proteins / immunology
  • Protein Conformation, beta-Strand

Substances

  • Antigens, Plant
  • MALD1 protein, Malus domestica
  • Plant Proteins