8TLD
Structure of the IL-5 Signaling Complex
8TLD の概要
| エントリーDOI | 10.2210/pdb8tld/pdb |
| EMDBエントリー | 41367 |
| 分子名称 | Cytokine receptor common subunit beta, Interleukin-5, Interleukin-5 receptor subunit alpha, ... (4 entities in total) |
| 機能のキーワード | il-5, cytokine, receptor, signaling protein |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 5 |
| 化学式量合計 | 241525.82 |
| 構造登録者 | |
| 主引用文献 | Caveney, N.A.,Rodriguez, G.E.,Pollmann, C.,Meyer, T.,Borowska, M.T.,Wilson, S.C.,Wang, N.,Xiang, X.,Householder, K.D.,Tao, P.,Su, L.L.,Saxton, R.A.,Piehler, J.,Garcia, K.C. Structure of the interleukin-5 receptor complex exemplifies the organizing principle of common beta cytokine signaling. Mol.Cell, 84:1995-2005.e7, 2024 Cited by PubMed Abstract: Cytokines regulate immune responses by binding to cell surface receptors, including the common subunit beta (βc), which mediates signaling for GM-CSF, IL-3, and IL-5. Despite known roles in inflammation, the structural basis of IL-5 receptor activation remains unclear. We present the cryo-EM structure of the human IL-5 ternary receptor complex, revealing architectural principles for IL-5, GM-CSF, and IL-3. In mammalian cell culture, single-molecule imaging confirms hexameric IL-5 complex formation on cell surfaces. Engineered chimeric receptors show that IL-5 signaling, as well as IL-3 and GM-CSF, can occur through receptor heterodimerization, obviating the need for higher-order assemblies of βc dimers. These findings provide insights into IL-5 and βc receptor family signaling mechanisms, aiding in the development of therapies for diseases involving deranged βc signaling. PubMed: 38614096DOI: 10.1016/j.molcel.2024.03.023 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.6 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






