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
Hauptverfasser: Köck, Zoe, Schnelle, Kilian, Persechino, Margherita, Umbach, Simon, Schihada, Hannes, Januliene, Dovile, Parey, Kristian, Pockes, Steffen, Kolb, Peter, Dötsch, Volker, Möller, Arne, Hilger, Daniel, Bernhard, Frank
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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.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-024-46096-z