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-Structure paper
タイトル | Unveiling the structural mechanisms of nonpeptide ligand recognition and activation in human chemokine receptor CCR8. |
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ジャーナル・号・ページ | Sci Adv, Vol. 10, Issue 5, Page eadj7500, Year 2024 |
掲載日 | 2024年2月2日 |
著者 | Shan Jiang / Xi Lin / Lijie Wu / Ling Wang / Yiran Wu / Ziyi Xu / Fei Xu / |
PubMed 要旨 | The human CC chemokine receptor 8 (CCR8) is an emerging therapeutic target for cancer immunotherapy and autoimmune diseases. Understanding the molecular recognition of CCR8, particularly with ...The human CC chemokine receptor 8 (CCR8) is an emerging therapeutic target for cancer immunotherapy and autoimmune diseases. Understanding the molecular recognition of CCR8, particularly with nonpeptide ligands, is valuable for drug development. Here, we report three cryo-electron microscopy structures of human CCR8 complexed with G trimers in the ligand-free state or activated by nonpeptide agonists LMD-009 and ZK 756326. A conserved YYE motif in the orthosteric binding pocket is shown to play a crucial role in the chemokine and nonpeptide ligand recognition. Structural and functional analyses indicate that the lack of conservation in Y114 and Y172 among the CC chemokine receptors could potentially contribute to the selectivity of the nonpeptide ligand binding to CCR8. These findings present the characterization of the molecular interaction between a nonpeptide agonist and a chemokine receptor, aiding the development of therapeutics targeting related diseases through a structure-based approach. |
リンク | Sci Adv / PubMed:38306437 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 2.96 - 3.3 Å |
構造データ | EMDB-37207, PDB-8kfx: EMDB-37208, PDB-8kfy: EMDB-37209, PDB-8kfz: |
化合物 |
ChemComp-OS9:
ChemComp-OXF: |
由来 |
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キーワード | SIGNALING PROTEIN / GPCR Gi Agonist / GPCR (Gタンパク質共役受容体) / Gi / Agonist (アゴニスト) / Complex |