Beyond dimerization:: A membrane-dependent activation model for interleukin-4 receptor-mediated signalling

被引:18
作者
Weidemann, Thomas
Hoefinger, Siegfried
Mueller, Kurt
Auer, Manfred
机构
[1] NIBR, A-1235 Vienna, Austria
[2] Michigan Technol Univ, Dept Phys, Houghton, MI 49931 USA
关键词
interleukin-4; receptor; WSXWS motif; signal transduction; membrane biophysics; free energy perturbation; GROWTH-HORMONE RECEPTOR; HIGH-AFFINITY INTERACTION; ERYTHROPOIETIN RECEPTOR; LIGAND-BINDING; ALPHA-CHAIN; T-CELLS; EXTRACELLULAR DOMAIN; CYTOKINE RECEPTORS; CYTOSOLIC DOMAINS; CRYSTAL-STRUCTURE;
D O I
10.1016/j.jmb.2006.11.095
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
Class I cytokine receptors efficiently transfer activation signals from the extracellular space to the cytoplasm and play a dominant role in growth control and differentiation of human tissues. Although a significant body of literature is devoted to this topic, a consistent mechanistic picture for receptor activation in the membrane environment is still missing. Using the interleukin-4 receptor (IL-4R) as an example, we propose that the membrane-proximal stem-loop of the extracellular domains contains pivotal elements of a rotational switch. Interfacial energies of amino acid side-chains contained in the highly conserved WSXWS at the surface of the lipid bilayer suggest a new functional role for this motif. A generic activation mechanism for this receptor class is presented, which may impact the design of a new generation of biophysical assay systems. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1365 / 1373
页数:9
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