Uncovering the triggers for GPCR activation using solid-state NMR spectroscopy

作者：Kimata Naoki; Reeves Philip J; Smith Steven O^*

来源：Journal of Magnetic Resonance, 2015, 253: 111-118.

DOI：10.1016/j.jmr.2014.12.014

• Solid-state NMR spectroscopy
• G protein-coupled receptor
• Magic angle spinning

G protein-coupled receptors (GPCRs) span cell membranes with seven transmembrane helices and respond to a diverse array of extracellular signals. Crystal structures of GPCRs have provided key insights into the architecture of these receptors and the role of conserved residues. However, the question of how ligand binding induces the conformational changes that are essential for activation remains largely unanswered. Since the extracellular sequences and structures of GPCRs are not conserved between receptor subfamilies, it is likely that the initial molecular triggers for activation vary depending on the specific type of ligand and receptor. In this article, we describe NMR studies on the rhodopsin subfamily of GPCRs and propose a mechanism for how retinal isomerization switches the receptor to the active conformation. These results suggest a general approach for determining the triggers for activation in other GPCR subfamilies using NMR spectroscopy.

• 出版日期2015-4