| Literature DB >> 31257107 |
Jiwan Ge1, Soumya G Remesh2, Michal Hammel2, Si Pan1, Andrew D Mahan3, Shuying Wang4, Xinquan Wang5.
Abstract
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.Entities:
Keywords: IL-1 receptor family; dual-luciferase reporter assay; inter-domain flexibility; minimal ensemble search; signal transduction; small-angle X-ray scattering (SAXS)
Year: 2019 PMID: 31257107 PMCID: PMC6687543 DOI: 10.1016/j.str.2019.05.011
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006