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Crystal structure of the mouse interleukin-3 β-receptor: insights into interleukin-3 binding and receptor activation

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Carr, Paul D
Ewans, Cameron
Dai, Jin
Ollis, David
Murphy, James M
Jackson, Colin
Young, I M

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Portland Press

Abstract

Interleukin-3 (IL-3) is a cytokine secreted by mast cells and activated T-cells known to be an important regulator of differentiation, survival, proliferation and activation of a range of haemopoietic lineages. The effects of IL-3 on target cells are mediated by a transmembrane receptor system composed of a cytokine-specific α-subunit and a β-subunit, the principal signalling entity. In the mouse, two β-subunits have co-evolved: a common β-subunit (βc) shared between IL-3 and the related cytokines IL-5 and granulocyte/macrophage colony-stimulating factor (GM-CSF); and an IL-3-specific β-subunit (βIL-3). βIL-3differs from βc in its specificity for IL-3 and its capacity to bind IL-3 directly in the absence of an α-subunit, and, in the absence of structural information, the basis for these properties has remained enigmatic. In the present study, we have solved the crystal structure of the βIL-3ectodomain at 3.45 A˚ (1 A˚ = 0.1 nm) resolution. This structure provides the first evidence that βIL-3adopts an arch-shaped intertwined homodimer with similar topology to the paralogous βc structure. In contrast with apo-βc, however, the ligand-binding interface of βIL-3appears to preexist in a conformation receptive to IL-3 engagement. Molecular modelling of the IL-3-βIL-3interface, in conjunctionwith previous mutational studies, suggests that divergent evolution of both βIL-3and IL-3 underlies their unique capacity for direct interaction and specificity.

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Biochemical Journal

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Restricted until

2037-12-31