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Elucidating ligand-bound structures of membrane proteins using solid-state NMR spectroscopy

Authors :
Massachusetts Institute of Technology. Department of Chemistry
Elkins, Matthew Ryan
Hong, Mei
Massachusetts Institute of Technology. Department of Chemistry
Elkins, Matthew Ryan
Hong, Mei
Source :
PMC
Publication Year :
2020

Abstract

Magic-angle-spinning (MAS) solid-state NMR spectroscopy is a versatile technique to elucidate functionally important protein–ligand interactions in lipid membranes. Here, we review recent solid-state NMR studies of membrane protein interactions with cholesterol, lipids, transported substrates, and peptide ligands. These studies are conducted in synthetic or native lipid bilayers to provide an accurate environment for ligand binding. The solid-state NMR approaches include multinuclear detection to gain comprehensive structural information, distance measurements to locate ligand-binding sites, and dynamic nuclear polarization and 1 H detection to enhance spectral sensitivity. These studies provide novel insights into the mechanisms of virus budding, virus entry into cells, transmembrane signaling, substrate transport, antibacterial action, and many other biological processes.<br />National Institutes of Health (U.S.) (Grant GM088204)

Details

Database :
OAIster
Journal :
PMC
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1239994375
Document Type :
Electronic Resource