The IgE network is associated with immunity to parasitic infection and with the allergic response. The interaction of IgE antibodies with two receptors, FceRI and CD23, couples the diversity of the IgE repertoire to effector cells of the immune system. Effector functions triggered by IgE:antigen complexes include the activation of mast cells, basophils and eosinophils, the feedback regulation of IgE production and the introduction of antigen into MHC class II antigen presentation pathways. We have previously elucidated the crystal structures of the ectodomains of the high affinity IgE receptor (FceRIa), the IgE-Fc Ce3/Ce4 domains and the complex of the IgE-Fc bound to FceRIa. The structures have provided new insights into the interactions between these two proteins and raised additional questions relevant to our understanding of IgE function and the development of new therapeutic approaches to treating allergic diseases.
The aims of this proposal are to investigate new leads for developing inhibitors of the IgE-Fc:FceRIa interaction, based on previous structural and biochemical observations. In addition, the role of IgE-Fc conformational transitions in binding interactions with both FceRI and CD23 will be explored using mutagenesis and X-ray crystallography. Further crystallographic studies of the interaction of IgE with both of its receptors will be pursued, in an effort to elucidate basic new mechanisms in antibody biology, with relevance to our understanding and treatment of atopic diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37AI038972-09
Application #
6750190
Study Section
Special Emphasis Panel (ZRG1-IMS (02))
Program Officer
Bocek, Petr
Project Start
1996-06-01
Project End
2006-05-31
Budget Start
2004-06-01
Budget End
2005-05-31
Support Year
9
Fiscal Year
2004
Total Cost
$294,000
Indirect Cost
Name
Northwestern University at Chicago
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
160079455
City
Evanston
State
IL
Country
United States
Zip Code
60201
Eggel, Alexander; Baravalle, Günther; Hobi, Gabriel et al. (2014) Accelerated dissociation of IgE-Fc?RI complexes by disruptive inhibitors actively desensitizes allergic effector cells. J Allergy Clin Immunol 133:1709-19.e8
Kim, Beomkyu; Tarchevskaya, Svetlana S; Eggel, Alexander et al. (2012) A time-resolved fluorescence resonance energy transfer assay suitable for high-throughput screening for inhibitors of immunoglobulin E-receptor interactions. Anal Biochem 431:84-9
Kim, Beomkyu; Eggel, Alexander; Tarchevskaya, Svetlana S et al. (2012) Accelerated disassembly of IgE-receptor complexes by a disruptive macromolecular inhibitor. Nature 491:613-7
Wurzburg, Beth A; Jardetzky, Theodore S (2009) Conformational flexibility in immunoglobulin E-Fc 3-4 revealed in multiple crystal forms. J Mol Biol 393:176-90