A structural insight into the reorientation of transmembrane domains 3 and 5 during family A G protein-coupled receptor activation
| Autor: | Saskia Nijmeijer, Rob Leurs, Ivan R. Torrecillas, Leonardo Pardo, Remko A. Bakker, Kamonchanok Sansuk, Xavier Deupi, Aldo Jongejan |
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| Rok vydání: | 2010 |
| Předmět: |
Pharmacology
Models Molecular COS cells Stereochemistry Mutagenesis Membrane Proteins Plasma protein binding Biology Receptors G-Protein-Coupled Transmembrane domain Helix COS Cells Chlorocebus aethiops Mutagenesis Site-Directed Molecular Medicine Animals Humans Sequence motif Receptor G protein-coupled receptor Protein Binding |
| Zdroj: | Molecular pharmacology. 79(2) |
| ISSN: | 1521-0111 |
| Popis: | Rearrangement of transmembrane domains (TMs) 3 and 5 after agonist binding is necessary for stabilization of the active state of class A G protein-coupled receptors (GPCRs). Using site-directed mutagenesis and functional assays, we provide the first evidence that the TAS(I/V) sequence motif at positions 3.37 to 3.40, highly conserved in aminergic receptors, plays a key role in the activation of the histamine H₁ receptor. By combining these data with structural information from X-ray crystallography and computational modeling, we suggest that Thr(3.37) interacts with TM5, stabilizing the inactive state of the receptor, whereas the hydrophobic side chain at position 3.40, highly conserved in the whole class A GPCR family, facilitates the reorientation of TM5. We propose that the structural change of TM5 during the process of GPCR activation involves a local Pro(5.50)-induced unwinding of the helix, acting as a hinge, and the highly conserved hydrophobic Ile(3.40) side chain, acting as a pivot. |
| Databáze: | OpenAIRE |
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