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-Structure paper
タイトル | GPCRs steer G and G selectivity via TM5-TM6 switches as revealed by structures of serotonin receptors. |
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ジャーナル・号・ページ | Mol Cell, Vol. 82, Issue 14, Page 2681-22695.e6, Year 2022 |
掲載日 | 2022年7月21日 |
![]() | Sijie Huang / Peiyu Xu / Dan-Dan Shen / Icaro A Simon / Chunyou Mao / Yangxia Tan / Huibing Zhang / Kasper Harpsøe / Huadong Li / Yumu Zhang / Chongzhao You / Xuekui Yu / Yi Jiang / Yan Zhang / David E Gloriam / H Eric Xu / ![]() ![]() ![]() |
PubMed 要旨 | Serotonin (or 5-hydroxytryptamine, 5-HT) is an important neurotransmitter that activates 12 different G protein-coupled receptors (GPCRs) through selective coupling of G, G or G proteins. The ...Serotonin (or 5-hydroxytryptamine, 5-HT) is an important neurotransmitter that activates 12 different G protein-coupled receptors (GPCRs) through selective coupling of G, G or G proteins. The structural basis for G protein subtype selectivity by these GPCRs remains elusive. Here, we report the structures of the serotonin receptors 5-HT, 5-HT, and 5-HT with G, and 5-HT with G. The structures reveal that transmembrane helices TM5 and TM6 alternate lengths as a macro-switch to determine receptor's selectivity for G and G, respectively. We find that the macro-switch by the TM5-TM6 length is shared by class A GPCR-G protein structures. Furthermore, we discover specific residues within TM5 and TM6 that function as micro-switches to form specific interactions with G or G. Together, these results present a common mechanism of G versus G protein coupling selectivity or promiscuity by class A GPCRs and extend the basis of ligand recognition at serotonin receptors. |
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手法 | EM (単粒子) |
解像度 | 3.1 - 3.3 Å |
構造データ | EMDB-33442, PDB-7xt8: EMDB-33443, PDB-7xt9: EMDB-33444, PDB-7xta: EMDB-33445, PDB-7xtb: EMDB-33446, PDB-7xtc: |
化合物 | ![]() ChemComp-CLR: ![]() ChemComp-PLM: ![]() ChemComp-SRO: ![]() ChemComp-8K3: |
由来 |
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![]() | MEMBRANE PROTEIN / GPCR / serotonin receptor / 5-HT / 5-HT4 receptor / signaling complex / cryo-EM structure / ligand selectivity / G protein selectivity / structure-function relationships / 5-HT6 receptor / 5-HT7 receptor |