TY - JOUR
T1 - Secret of the major birch pollen allergen Bet v 1
T2 - Identification of the physiological ligand
AU - Von Loetzen, Christian Seutter
AU - Hoffmann, Thomas
AU - Hartl, Maximilian J.
AU - Schweimer, Kristian
AU - Schwab, Wilfried
AU - Rösch, Paul
AU - Hartl-Spiegelhauer, Olivia
PY - 2014/2/1
Y1 - 2014/2/1
N2 - 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- Osophoroside) 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.
AB - 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- Osophoroside) 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.
KW - Allergen
KW - Bet v 1
KW - NMR
KW - Quercetin-3-O-sophoroside(Q3OS)
UR - http://www.scopus.com/inward/record.url?scp=84892188196&partnerID=8YFLogxK
U2 - 10.1042/BJ20130413
DO - 10.1042/BJ20130413
M3 - Article
C2 - 24171862
AN - SCOPUS:84892188196
SN - 0264-6021
VL - 457
SP - 379
EP - 390
JO - Biochemical Journal
JF - Biochemical Journal
IS - 3
ER -