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-Structure paper
タイトル | Structures of the entire human opioid receptor family. |
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ジャーナル・号・ページ | Cell, Vol. 186, Issue 2, Page 413-427.e17, Year 2023 |
掲載日 | 2023年1月19日 |
著者 | Yue Wang / Youwen Zhuang / Jeffrey F DiBerto / X Edward Zhou / Gavin P Schmitz / Qingning Yuan / Manish K Jain / Weiyi Liu / Karsten Melcher / Yi Jiang / Bryan L Roth / H Eric Xu / |
PubMed 要旨 | Opioids are effective analgesics, but their use is beset by serious side effects, including addiction and respiratory depression, which contribute to the ongoing opioid crisis. The human opioid ...Opioids are effective analgesics, but their use is beset by serious side effects, including addiction and respiratory depression, which contribute to the ongoing opioid crisis. The human opioid system contains four opioid receptors (μOR, δOR, κOR, and NOPR) and a set of related endogenous opioid peptides (EOPs), which show distinct selectivity toward their respective opioid receptors (ORs). Despite being key to the development of safer analgesics, the mechanisms of molecular recognition and selectivity of EOPs to ORs remain unclear. Here, we systematically characterize the binding of EOPs to ORs and present five structures of EOP-OR-G complexes, including β-endorphin- and endomorphin-bound μOR, deltorphin-bound δOR, dynorphin-bound κOR, and nociceptin-bound NOPR. These structures, supported by biochemical results, uncover the specific recognition and selectivity of opioid peptides and the conserved mechanism of opioid receptor activation. These results provide a structural framework to facilitate rational design of safer opioid drugs for pain relief. |
リンク | Cell / PubMed:36638794 |
手法 | EM (単粒子) |
解像度 | 3.0 - 3.28 Å |
構造データ | EMDB-28907, PDB-8f7q: EMDB-28908, PDB-8f7r: EMDB-28909, PDB-8f7s: EMDB-28911, PDB-8f7w: EMDB-28912, PDB-8f7x: |
化合物 | ChemComp-CLR: ChemComp-PLM: |
由来 |
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キーワード | SIGNALING PROTEIN / mu opioid receptor / G protein coupled receptor / beta-endorphin / endomorphin / delta opioid receptor / deltorphin / kappa opioid receptor / dynorphin |