Ligand Binding-Induced Structural Changes in the M <sub/>2</sub> Muscarinic Acetylcholine Receptor Revealed by Vibrational Spectroscopy

摘要： M2 muscarinic acetylcholine receptor (M2R) is a prototypical G protein-coupled receptor (GPCR) that responds to acetylcholine and mediates various cellular responses in the nervous system. Here, we used Attenuated Total Reflection-Fourier Transform Infrared (ATR-FTIR) spectroscopy analyses on M2R reconstituted in lipid membrane to understand the molecular mechanism behind the ligand binding-induced conformational changes. Upon agonist binding, M2R shows large spectral change of amide-I band corresponding to backbone C=O stretch, which likely connects with the receptor activation in lipid environment. These results pave the way to probe effects of different ligand binding on GPCRs using vibrational spectroscopy.