Evaluation of Different Glycoforms of Honeybee Venom Major Allergen Phospholipase A2 (Api m 1) Produced in Insect Cells

Simon      Blank; Yvonne      Michel; Henning      Seismann; Melanie      Plum; Kerstin      Greunke; Thomas      Grunwald; Reinhard      Bredehorst; Markus      Ollert; Ingke      Braren; Edzard      Spillner

doi:10.2174/092986611794653923

Abstract

Allergic reactions to hymenoptera stings are one of the major reasons for IgE-mediated anaphylaxis. However, proper diagnosis using venom extracts is severely affected by molecular cross-reactivity. In this study recombinant honeybee venom major allergen phospholipase A2 (Api m 1) was produced for the first time in insect cells. Using baculovirus infection of different insect cell lines allergen versions providing a varying degree of cross-reactive carbohydrate determinants as well as a non glycosylated variant could be obtained as secreted soluble proteins in high yields. The resulting molecules were analyzed for their glycosylation and proved to show advantageous properties regarding cross-reactivity in sIgE-based assays. Additionally, in contrast to the enzymatically active native protein the inactivated allergen did not induce IgE-independent effector cell activation. Thus, insect cell-derived recombinant Api m 1 with defined CCD phenotypes might provide further insights into hymenoptera venom IgE reactivities and contribute to an improved diagnosis of hymenoptera venom allergy.

Keywords: Allergen, baculovirus, carbohydrates, cross-reactivity, honeybee, phospholipase, recombinant allergen, venom allergy, Glycoforms, Honeybee Venom, Phospholipase A2, hymenoptera stings, IgE-mediated anaphylaxis, CCD phenotypes, hymenoptera venom, Site Directed Mutagenesis, Recombinant Baculovirus, RBL-SX38, agglutinin, HBV acid phosphatase, MUXF-HASAllergen, baculovirus, carbohydrates, cross-reactivity, honeybee, phospholipase, recombinant allergen, venom allergy, Glycoforms, Honeybee Venom, Phospholipase A2, hymenoptera stings, IgE-mediated anaphylaxis, CCD phenotypes, hymenoptera venom, Site Directed Mutagenesis, Recombinant Baculovirus, RBL-SX38, agglutinin, HBV acid phosphatase, MUXF-HAS