Secret of the major birch pollen allergen Bet v 1: identification of the physiological ligand

被引:77
|
作者
Seutter von Loetzen, Christian [1 ,2 ]
Hoffmann, Thomas [3 ]
Hartl, Maximilian J. [1 ,2 ]
Schweimer, Kristian [1 ,2 ]
Schwab, Wilfried [3 ]
Roesch, Paul [1 ,2 ]
Hartl-Spiegelhauer, Olivia [1 ,2 ]
机构
[1] Univ Bayreuth, Lehrstuhl Biopolymere, D-95447 Bayreuth, Germany
[2] Univ Bayreuth, Forschungszentrum Biomakromol, D-95447 Bayreuth, Germany
[3] Tech Univ Munich, D-85354 Freising Weihenstephan, Germany
关键词
allergen; Bet v 1; NMR; quercetin-3-O-sophoroside (Q3OS); PATHOGENESIS-RELATED PROTEINS; LECTIN-CARBOHYDRATE INTERACTIONS; FLAVONOL; 3-O-GALACTOSYLTRANSFERASE; BIOLOGICAL FUNCTION; CROSS-REACTIVITY; IGE REACTIVITY; FOOD ALLERGENS; IN-VITRO; X-RAY; BET-V-1;
D O I
10.1042/BJ20130413
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The major birch pollen allergen Bet v 1 is the main elicitor of airborne type I allergies and belongs to the PR-10 family (pathogenesis-related proteins 10). Bet v 1 is the most extensively studied allergen, and is well characterized at a biochemical and immunological level; however, its physiological function remains elusive. In the present study, we identify Q3OS (quercetin-3-O-sophoroside) as the natural ligand of Bet v 1. We isolated Q3OS bound to Bet v 1 from mature birch pollen and confirmed its binding by reconstitution of the Bet v 1-Q3OS complex. Fluorescence and UV visible spectroscopy experiments, as well as HSQC (heteronuclear single-quantum coherence) titration, and the comparison with model compounds, such as quercetin, indicated the specificity of Q3OS binding. Elucidation of the binding site by NMR combined with a computational model resulted in a more detailed understanding and shed light on the physiological function of Bet v 1. We postulate that the binding of Q3OS to Bet v 1 plays an important, but as yet unclear, role during the inflammation response and Bet v 1 recognition by IgE.
引用
收藏
页码:379 / 390
页数:12
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