Ministry of Education Key Laboratory of Protein Science, Beijing Advanced Innovation Center for Structural Biology, Beijing Frontier Research Center for Biological Structure, Collaborative Innovation Center for Biotherapy, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Molecular Biophysics and Integrated Bioimaging, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
Structure. 2019 Aug 6;27(8):1296-1307.e5. doi: 10.1016/j.str.2019.05.011. Epub 2019 Jun 27.
The interleukin 1 (IL-1) receptor family, whose members contain three immunoglobulin-like domains (D1-D3) in the extracellular region, is responsible for transmitting pleiotropic signals of IL-1 cytokines. The inter-domain flexibility of IL-1 receptors and its functional roles have not been fully elucidated. In this study, we used small-angle X-ray scattering to show that ligand-binding primary receptors and co-receptors in the family all have inherent inter-domain flexibility due to the D2/D3 linker. Variants of the IL-1RAcP and IL-18Rβ co-receptors with mutated D2/D3 linkers cannot form a cytokine-receptor complex and mediate signaling. Our analysis further revealed that these mutated co-receptors exhibited a changed conformational ensemble, suggesting that loss of function is due to the alteration of receptor dynamics. Taken together, our results demonstrate that the D2/D3 linker is a critical functional determinant of IL-1 receptor and underscore the important roles of the inter-domain flexibility in cytokine/receptor binding and signaling.
白细胞介素 1 (IL-1) 受体家族,其成员在细胞外区域包含三个免疫球蛋白样结构域 (D1-D3),负责传递 IL-1 细胞因子的多种信号。IL-1 受体的结构域间灵活性及其功能作用尚未完全阐明。在这项研究中,我们使用小角度 X 射线散射表明,家族中的配体结合主要受体和共受体由于 D2/D3 接头都具有固有结构域间灵活性。具有突变 D2/D3 接头的 IL-1RAcP 和 IL-18Rβ 共受体变体不能形成细胞因子-受体复合物并介导信号转导。我们的分析进一步表明,这些突变共受体表现出改变的构象整体,表明功能丧失是由于受体动力学的改变。总之,我们的结果表明 D2/D3 接头是 IL-1 受体的关键功能决定因素,并强调了结构域间灵活性在细胞因子/受体结合和信号转导中的重要作用。