A propofol binding site on mammalian GABAA receptors identified by photolabeling
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Anesthetics target interfacial transmembrane sites in nicotinic acetylcholine receptorsCrystal structure of a human GABAA receptorMutations at beta N265 in γ-aminobutyric acid type A receptors alter both binding affinity and efficacy of potent anestheticsClick Chemistry Reagent for Identification of Sites of Covalent Ligand Incorporation in Integral Membrane Proteins.Photoaffinity Labeling of Pentameric Ligand-Gated Ion Channels: A Proteomic Approach to Identify Allosteric Modulator Binding Sites.Curcumol allosterically modulates GABA(A) receptors in a manner distinct from benzodiazepines.Analogues of etomidate: modifications around etomidate's chiral carbon and the impact on in vitro and in vivo pharmacologyMultiple propofol-binding sites in a γ-aminobutyric acid type A receptor (GABAAR) identified using a photoreactive propofol analog.Multiple Non-Equivalent Interfaces Mediate Direct Activation of GABAA Receptors by Propofol.Volatile anesthetics inhibit sodium channels without altering bulk lipid bilayer properties.Comparative pharmacology of flatworm and roundworm glutamate-gated chloride channels: Implications for potential anthelmintics.The neurosteroid 5β-pregnan-3α-ol-20-one enhances actions of etomidate as a positive allosteric modulator of α1β2γ2L GABAA receptorsGeneration of recombinant antibodies to rat GABAA receptor subunits by affinity selection on synthetic peptidesDodecyl maltopyranoside enabled purification of active human GABA type A receptors for deep and direct proteomic sequencingPropofol inhibits SIRT2 deacetylase through a conformation-specific, allosteric site.Phosphatidylinositol 4,5-bisphosphate depletion fails to affect neurosteroid modulation of GABAA receptor function.Mutational Analysis of the Putative High-Affinity Propofol Binding Site in Human β3 Homomeric GABAA Receptors.Discovery of allosteric modulators for GABAA receptors by ligand-directed chemistry.Metabolomics profiling of pre-and post-anesthesia plasma samples of colorectal patients obtained via Ficoll separation.Propofol requirement for induction of unconsciousness is reduced in patients with Parkinson's disease: a case control study.A Cysteine Substitution Probes β3H267 Interactions with Propofol and Other Potent Anesthetics in α1β3γ2L γ-Aminobutyric Acid Type A ReceptorsNovel positive allosteric modulators of GABAA receptors with anesthetic activity.Inter- and Intra-Subunit Butanol/Isoflurane Sites of Action in the Human Glycine Receptor.Role for the propofol hydroxyl in anesthetic protein target molecular recognition.A Novel Bifunctional Alkylphenol Anesthetic Allows Characterization of γ-Aminobutyric Acid, Type A (GABAA), Receptor Subunit Binding Selectivity in Synaptosomes.Neonatal Propofol and Etomidate Exposure Enhance Inhibitory Synaptic Transmission in Hippocampal Cornus Ammonis 1 Pyramidal Neurons.Mechanisms revealed through general anesthetic photolabeling.Noncompetitive Inhibition of 5-HT3 Receptors by Citral, Linalool, and Eucalyptol Revealed by Nonlinear Mixed-Effects Modeling.Development of Photoactivatable Allosteric Modulators for the Chemokine Receptor CXCR3.Orthosteric- versus allosteric-dependent activation of the GABAA receptor requires numerically distinct subunit level rearrangements.The actions of drug combinations on the GABAA receptor manifest as curvilinear isoboles of additivity.Differential Potency of 2,6-Dimethylcyclohexanol Isomers for Positive Modulation of GABAA Receptor Currents.Shedding Light on Anesthetic Mechanisms: Application of Photoaffinity Ligands.Mapping General Anesthetic Sites in Heteromeric γ-Aminobutyric Acid Type A Receptors Reveals a Potential For Targeting Receptor Subtypes.Structural mechanisms of activation and desensitization in neurotransmitter-gated ion channels.Identification of a putative binding site critical for general anesthetic activation of TRPA1.Detergents: Friends not foes for high-performance membrane proteomics toward precision medicine.Structural Studies of GABAA Receptor Binding Sites: Which Experimental Structure Tells us What?Identification of amino acids involved in histamine potentiation of GABA A receptors.Photoaffinity labeling the propofol binding site in GLIC.
P2860
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P2860
A propofol binding site on mammalian GABAA receptors identified by photolabeling
description
2013 nî lūn-bûn
@nan
2013 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
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name
A propofol binding site on mammalian GABAA receptors identified by photolabeling
@ast
A propofol binding site on mammalian GABAA receptors identified by photolabeling
@en
A propofol binding site on mammalian GABAA receptors identified by photolabeling
@nl
type
label
A propofol binding site on mammalian GABAA receptors identified by photolabeling
@ast
A propofol binding site on mammalian GABAA receptors identified by photolabeling
@en
A propofol binding site on mammalian GABAA receptors identified by photolabeling
@nl
prefLabel
A propofol binding site on mammalian GABAA receptors identified by photolabeling
@ast
A propofol binding site on mammalian GABAA receptors identified by photolabeling
@en
A propofol binding site on mammalian GABAA receptors identified by photolabeling
@nl
P2093
P2860
P50
P356
P1476
A propofol binding site on mammalian GABAA receptors identified by photolabeling
@en
P2093
Christopher J Edge
Edward H Smith
Erhard Hohenester
Grace M S Yip
Karoline Fuchs
R Reid Townsend
Robert Dickinson
Zi-Wei Chen
P2860
P2888
P304
P356
10.1038/NCHEMBIO.1340
P577
2013-09-22T00:00:00Z