Molecular cloning and expression of icarapin, a novel IgE-binding bee venom protein

FEBS Lett. 2006 Sep 4;580(20):4895-9. doi: 10.1016/j.febslet.2006.08.005. Epub 2006 Aug 10.

Abstract

The 1045bp full-length cDNA sequence of a new bee venom component was obtained by rapid amplification of cDNA ends. The 672bp coding sequence corresponds to a protein with a signal peptide and multiple carbohydrate binding sites, and it was named icarapin. It has the new consensus sequence N-[TS]-T-S-[TV]-x-K-[VI](2)-[DN]-G-H-x-V-x-I-N-[ED]-T-x-Y-x-[DHK]-x(2,6)- [STA]-[VLFI]-x-[KR]-V-R-[VLI]-[IV]-[DN]-V-x-P. At least two transcript variants were found. Recombinant icarapin was tested for recognition by IgE antibodies and gave a positive dot blot with sera from 4 out of 5 bee venom allergic patients, all beekeepers. Indirect immunofluorescent staining localized the protein in the cuticular lining of the venom duct.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Bee Venoms / chemistry*
  • Bee Venoms / immunology
  • Bees / anatomy & histology
  • Bees / chemistry
  • Bees / metabolism
  • Carrier Proteins / chemistry*
  • Carrier Proteins / immunology
  • Cloning, Molecular
  • Humans
  • Hypersensitivity, Immediate / immunology
  • Immunoglobulin E / metabolism*
  • Insect Proteins / genetics
  • Insect Proteins / isolation & purification*
  • Insect Proteins / metabolism*
  • Molecular Sequence Data
  • Rabbits
  • Sequence Alignment

Substances

  • Bee Venoms
  • Carrier Proteins
  • Insect Proteins
  • icarapin protein, Apis mellifera
  • Immunoglobulin E