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-Structure paper
タイトル | Molecular Basis for Hormone Recognition and Activation of Corticotropin-Releasing Factor Receptors. |
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ジャーナル・号・ページ | Mol Cell, Vol. 77, Issue 3, Page 669-680.e4, Year 2020 |
掲載日 | 2020年2月6日 |
著者 | Shanshan Ma / Qingya Shen / Li-Hua Zhao / Chunyou Mao / X Edward Zhou / Dan-Dan Shen / Parker W de Waal / Peng Bi / Chuntao Li / Yi Jiang / Ming-Wei Wang / Patrick M Sexton / Denise Wootten / Karsten Melcher / Yan Zhang / H Eric Xu / |
PubMed 要旨 | Corticotropin-releasing factor (CRF) and the three related peptides urocortins 1-3 (UCN1-UCN3) are endocrine hormones that control the stress responses by activating CRF1R and CRF2R, two members of ...Corticotropin-releasing factor (CRF) and the three related peptides urocortins 1-3 (UCN1-UCN3) are endocrine hormones that control the stress responses by activating CRF1R and CRF2R, two members of class B G-protein-coupled receptors (GPCRs). Here, we present two cryoelectron microscopy (cryo-EM) structures of UCN1-bound CRF1R and CRF2R with the stimulatory G protein. In both structures, UCN1 adopts a single straight helix with its N terminus dipped into the receptor transmembrane bundle. Although the peptide-binding residues in CRF1R and CRF2R are different from other members of class B GPCRs, the residues involved in receptor activation and G protein coupling are conserved. In addition, both structures reveal bound cholesterol molecules to the receptor transmembrane helices. Our structures define the basis of ligand-binding specificity in the CRF receptor-hormone system, establish a common mechanism of class B GPCR activation and G protein coupling, and provide a paradigm for studying membrane protein-lipid interactions for class B GPCRs. |
リンク | Mol Cell / PubMed:32004470 |
手法 | EM (単粒子) |
解像度 | 2.8 - 3.0 Å |
構造データ | EMDB-20284, PDB-6pb0: EMDB-20285, PDB-6pb1: |
化合物 | ChemComp-CLR: ChemComp-PLM: |
由来 |
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キーワード | SIGNALING PROTEIN / Corticotropin-releasing factor 1 receptor / urocortins1 / Gs protein / GPCR / Corticotropin-releasing factor 2 receptor |