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-Structure paper
タイトル | Cryo-EM structure of G-protein-coupled receptor GPR17 in complex with inhibitory G protein. |
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ジャーナル・号・ページ | MedComm (2020), Vol. 3, Issue 4, Page e159, Year 2022 |
掲載日 | 2022年9月10日 |
著者 | Fang Ye / Thian-Sze Wong / Geng Chen / Zhiyi Zhang / Binghao Zhang / Shiyi Gan / Wei Gao / Jiancheng Li / Zhangsong Wu / Xin Pan / Yang Du / |
PubMed 要旨 | GPR17 is a class A orphan G protein-coupled receptor (GPCR) expressed in neurons and oligodendrocyte progenitors of the central nervous system (CNS). The signalling of GPR17 occurs through the ...GPR17 is a class A orphan G protein-coupled receptor (GPCR) expressed in neurons and oligodendrocyte progenitors of the central nervous system (CNS). The signalling of GPR17 occurs through the heterotrimeric Gi, but its activation mechanism is unclear. Here, we employed cryo-electron microscopy (cryo-EM) technology to elucidate the structure of activated GPR17-Gi complex. The 3.02 Å resolution structure, together with mutagenesis studies, revealed that the extracellular loop2 of GPR17 occupied the orthosteric binding pocket to promote its self-activation. The active GPR17 carried several typical microswitches like other class A GPCRs. Moreover, the Gi interacted with the key residues of transmembrane helix 3 (TM3), the amphipathic helix 8 (Helix8), and intracellular loops 3 (ICL3) in GPR17 to engage in the receptor core. In summary, our results highlight the activation mechanism of GPR17 from the structural basis. Elucidating the structural and activation mechanism of GPR17 may facilitate the pharmacological intervention for acute/chronic CNS injury. |
リンク | MedComm (2020) / PubMed:36105372 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 3.02 Å |
構造データ | EMDB-33682, PDB-7y89: |
由来 |
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キーワード | MEMBRANE PROTEIN / classA GPCR / complex |