Cryo-EM structure of cell-free synthesized human histamine 2 receptor/Gs complex in nanodisc environment
Here we describe the cryo-electron microscopy structure of the human histamine 2 receptor (H 2 R) in an active conformation with bound histamine and in complex with G s heterotrimeric protein at an overall resolution of 3.4 Å. The complex was generated by cotranslational insertion of the receptor in...
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Veröffentlicht in: | Nature communications 2024-02, Vol.15 (1), p.1831-1831, Article 1831 |
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Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Here we describe the cryo-electron microscopy structure of the human histamine 2 receptor (H
2
R) in an active conformation with bound histamine and in complex with G
s
heterotrimeric protein at an overall resolution of 3.4 Å. The complex was generated by cotranslational insertion of the receptor into preformed nanodisc membranes using cell-free synthesis in
E
.
coli
lysates. Structural comparison with the inactive conformation of H
2
R and the inactive and G
q
-coupled active state of H
1
R together with structure-guided functional experiments reveal molecular insights into the specificity of ligand binding and G protein coupling for this receptor family. We demonstrate lipid-modulated folding of cell-free synthesized H
2
R, its agonist-dependent internalization and its interaction with endogenously synthesized H
1
R and H
2
R in HEK293 cells by applying a recently developed nanotransfer technique.
The study describes the molecular structure of the human histamine 2 receptor in active conformation and in complex with G
s
heterotrimer, synthesized in a cell-free system and co-translationally inserted into preformed nanodiscs. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-024-46096-z |