Literature DB >> 31488329

Agonist Selectivity and Ion Permeation in the α3β4 Ganglionic Nicotinic Receptor.

Anant Gharpure1, Jinfeng Teng1, Yuxuan Zhuang2, Colleen M Noviello1, Richard M Walsh1, Rico Cabuco1, Rebecca J Howard2, Nurulain T Zaveri3, Erik Lindahl4, Ryan E Hibbs5.   

Abstract

Nicotinic acetylcholine receptors are pentameric ion channels that mediate fast chemical neurotransmission. The α3β4 nicotinic receptor subtype forms the principal relay between the central and peripheral nervous systems in the autonomic ganglia. This receptor is also expressed focally in brain areas that affect reward circuits and addiction. Here, we present structures of the α3β4 nicotinic receptor in lipidic and detergent environments, using functional reconstitution to define lipids appropriate for structural analysis. The structures of the receptor in complex with nicotine, as well as the α3β4-selective ligand AT-1001, complemented by molecular dynamics, suggest principles of agonist selectivity. The structures further reveal much of the architecture of the intracellular domain, where mutagenesis experiments and simulations define residues governing ion conductance.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  addiction; cryo-EM; ganglionic; ligand-gated ion channel; lipids; nicotine; nicotinic receptor

Mesh:

Substances:

Year:  2019        PMID: 31488329      PMCID: PMC6842111          DOI: 10.1016/j.neuron.2019.07.030

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  90 in total

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  37 in total

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