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TitleStructural insights into galanin receptor signaling.
Journal, issue, pagesProc Natl Acad Sci U S A, Vol. 119, Issue 21, Page e2121465119, Year 2022
Publish dateMay 24, 2022
AuthorsWentong Jiang / Sanduo Zheng /
PubMed AbstractGalanin is a biologically active neuropeptide, and functions through three distinct G protein–coupled receptors (GPCRs), namely GALR1, GALR2, and GALR3. GALR signaling plays important roles in ...Galanin is a biologically active neuropeptide, and functions through three distinct G protein–coupled receptors (GPCRs), namely GALR1, GALR2, and GALR3. GALR signaling plays important roles in regulating various physiological processes such as energy metabolism, neuropathic pain, epileptic activity, and sleep homeostasis. GALR1 and GALR3 signal through the Gi/o pathway, whereas GALR2 signals mainly through the Gq/11 pathway. However, the molecular basis for galanin recognition and G protein selectivity of GALRs remains poorly understood. Here, we report the cryoelectron microscopy structures of the GALR1-Go and the GALR2-Gq complexes bound to the endogenous ligand galanin or spexin. The galanin peptide mainly adopts an alpha helical structure, which binds at the extracellular vestibule of the receptors, nearly parallel to the membrane plane without penetrating deeply into the receptor core. Structural analysis combined with functional studies reveals important structural determinants for the G protein selectivity of GALRs as well as other class A GPCRs. In addition, we show that the zinc ion is a negative allosteric regulator of GALR1 but not GALR2. Our studies provide insight into the mechanisms of G protein selectivity of GPCRs and highlight a potential function of the neuromodulator zinc ion as a modulator of GPCR signaling in the central nervous system.
External linksProc Natl Acad Sci U S A / PubMed:35594396 / PubMed Central
MethodsEM (single particle)
Resolution3.3 - 3.5 Å
Structure data

EMDB-33229, PDB-7xjj:
Cryo-EM structure of the galanin-bound GALR1-miniGo complex
Method: EM (single particle) / Resolution: 3.3 Å

EMDB-33230, PDB-7xjk:
Cryo-EM structure of the galanin-bound GALR2-miniGq complex
Method: EM (single particle) / Resolution: 3.3 Å

EMDB-33231, PDB-7xjl:
Cryo-EM structure of the spexin-bound GALR2-miniGq complex
Method: EM (single particle) / Resolution: 3.5 Å

Source
  • homo sapiens (human)
KeywordsSIGNALING PROTEIN / GPCR / Galanin receptor 1 / miniGo / galanin receptor 2 / mini-Gq / miniGq / spexin

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