Propofol Modulation of α1 Glycine Receptors Does Not Require a Structural Transition at Adjacent Subunits That Is Crucial to Agonist-Induced Activation-Reference-Cited by-同舟云学术

Propofol Modulation of α1 Glycine Receptors Does Not Require a Structural Transition at Adjacent Subunits That Is Crucial to Agonist-Induced Activation

Published:2013-09-17 Issue:11 Volume:4 Page:1469-1478
ISSN:1948-7193
Container-title:ACS Chemical Neuroscience
language:en
Short-container-title:ACS Chem. Neurosci.

Author:

Lynagh Timothy¹,Kunz Alexander¹,Laube Bodo¹

Affiliation:

1. Neurophysiology and Neurosensory Systems, Technische Universität Darmstadt, Schnittspahnstrasse 3, 64287 Darmstadt, Germany

Publisher

American Chemical Society (ACS)

Subject

Cell Biology,Cognitive Neuroscience,Physiology,Biochemistry,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/cn400134p

Reference58 articles.

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4. Decreased agonist affinity and chloride conductance of mutant glycine receptors associated with human hereditary hyperekplexia.

5. Mutation of an arginine residue in the human glycine receptor transforms β-alanine and taurine from agonists into competitive antagonists

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