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J Biol Chem
2013 Jun 14;28824:17420-31. doi: 10.1074/jbc.M113.464040.
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Propofol binding to the resting state of the gloeobacter violaceus ligand-gated ion channel (GLIC) induces structural changes in the inter- and intrasubunit transmembrane domain (TMD) cavities.
Ghosh B
,
Satyshur KA
,
Czajkowski C
.
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General anesthetics exert many of their CNS actions by binding to and modulating membrane-embedded pentameric ligand-gated ion channels (pLGICs). The structural mechanisms underlying how anesthetics modulate pLGIC function remain largely unknown. GLIC, a prokaryotic pLGIC homologue, is inhibited by general anesthetics, suggesting anesthetics stabilize a closed channel state, but in anesthetic-bound GLIC crystal structures the channel appears open. Here, using functional GLIC channels expressed in oocytes, we examined whether propofol induces structural rearrangements in the GLIC transmembrane domain (TMD). Residues in the GLIC TMD that frame intrasubunit and intersubunit water-accessible cavities were individually mutated to cysteine. We measured and compared the rates of modification of the introduced cysteines by sulfhydryl-reactive reagents in the absence and presence of propofol. Propofol slowed the rate of modification of L240C (intersubunit) and increased the rate of modification of T254C (intrasubunit), indicating that propofol binding induces structural rearrangements in these cavities that alter the local environment near these residues. Propofol acceleration of T254C modification suggests that in the resting state propofol does not bind in the TMD intrasubunit cavity as observed in the crystal structure of GLIC with bound propofol (Nury, H., Van Renterghem, C., Weng, Y., Tran, A., Baaden, M., Dufresne, V., Changeux, J. P., Sonner, J. M., Delarue, M., and Corringer, P. J. (2011) Nature 469, 428-431). In silico docking using a GLIC closed channel homology model suggests propofol binds to intersubunit sites in the TMD in the resting state. Propofol-induced motions in the intersubunit cavity were distinct from motions associated with channel activation, indicating propofol stabilizes a novel closed state.
Ahrens,
A transmembrane residue influences the interaction of propofol with the strychnine-sensitive glycine alpha1 and alpha1beta receptor.
2008, Pubmed
Ahrens,
A transmembrane residue influences the interaction of propofol with the strychnine-sensitive glycine alpha1 and alpha1beta receptor.
2008,
Pubmed
Akk,
Actions of anesthetics on excitatory transmitter-gated channels.
2008,
Pubmed
Baenziger,
3D structure and allosteric modulation of the transmembrane domain of pentameric ligand-gated ion channels.
2011,
Pubmed
Belelli,
The interaction of the general anesthetic etomidate with the gamma-aminobutyric acid type A receptor is influenced by a single amino acid.
1997,
Pubmed
,
Xenbase
Bocquet,
X-ray structure of a pentameric ligand-gated ion channel in an apparently open conformation.
2009,
Pubmed
Boileau,
Identification of transduction elements for benzodiazepine modulation of the GABA(A) receptor: three residues are required for allosteric coupling.
1999,
Pubmed
,
Xenbase
Borghese,
Sites of excitatory and inhibitory actions of alcohols on neuronal alpha2beta4 nicotinic acetylcholine receptors.
2003,
Pubmed
,
Xenbase
Brannigan,
Multiple binding sites for the general anesthetic isoflurane identified in the nicotinic acetylcholine receptor transmembrane domain.
2010,
Pubmed
Chen,
Evolutionarily conserved allosteric network in the Cys loop family of ligand-gated ion channels revealed by statistical covariance analyses.
2006,
Pubmed
Chen,
Anesthetic binding in a pentameric ligand-gated ion channel: GLIC.
2010,
Pubmed
Chiara,
Photoaffinity labeling the propofol binding site in GLIC.
2014,
Pubmed
,
Xenbase
Collins,
Nicotinic acetylcholine receptor transmembrane mutations convert ivermectin from a positive to a negative allosteric modulator.
2010,
Pubmed
,
Xenbase
Eswar,
Comparative protein structure modeling using Modeller.
2006,
Pubmed
Franks,
Molecular and cellular mechanisms of general anaesthesia.
1994,
Pubmed
Ghanouni,
Functionally different agonists induce distinct conformations in the G protein coupling domain of the beta 2 adrenergic receptor.
2001,
Pubmed
Hamouda,
Multiple transmembrane binding sites for p-trifluoromethyldiazirinyl-etomidate, a photoreactive Torpedo nicotinic acetylcholine receptor allosteric inhibitor.
2011,
Pubmed
Hanson,
Structural mechanisms underlying benzodiazepine modulation of the GABA(A) receptor.
2008,
Pubmed
,
Xenbase
Hasegawa,
Advances and pitfalls of protein structural alignment.
2009,
Pubmed
Hibbs,
Principles of activation and permeation in an anion-selective Cys-loop receptor.
2011,
Pubmed
Hilf,
Structure of a potentially open state of a proton-activated pentameric ligand-gated ion channel.
2009,
Pubmed
Hilf,
X-ray structure of a prokaryotic pentameric ligand-gated ion channel.
2008,
Pubmed
Howard,
Structural basis for alcohol modulation of a pentameric ligand-gated ion channel.
2011,
Pubmed
,
Xenbase
Huey,
A semiempirical free energy force field with charge-based desolvation.
2007,
Pubmed
Jayakar,
Identification of propofol binding sites in a nicotinic acetylcholine receptor with a photoreactive propofol analog.
2013,
Pubmed
Jha,
Acetylcholine receptor gating at extracellular transmembrane domain interface: the cys-loop and M2-M3 linker.
2007,
Pubmed
Karlin,
Substituted-cysteine accessibility method.
1998,
Pubmed
Kash,
Coupling of agonist binding to channel gating in the GABA(A) receptor.
2003,
Pubmed
Koltchine,
Agonist gating and isoflurane potentiation in the human gamma-aminobutyric acid type A receptor determined by the volume of a second transmembrane domain residue.
1999,
Pubmed
LeBard,
General anesthetics predicted to block the GLIC pore with micromolar affinity.
2012,
Pubmed
Lee,
Principal pathway coupling agonist binding to channel gating in nicotinic receptors.
2005,
Pubmed
Li,
Identification of a GABAA receptor anesthetic binding site at subunit interfaces by photolabeling with an etomidate analog.
2006,
Pubmed
Liu,
Binding site and affinity prediction of general anesthetics to protein targets using docking.
2012,
Pubmed
Mihic,
Sites of alcohol and volatile anaesthetic action on GABA(A) and glycine receptors.
1997,
Pubmed
,
Xenbase
Miller,
Binding, activation and modulation of Cys-loop receptors.
2010,
Pubmed
Morlock,
Different residues in the GABAA receptor benzodiazepine binding pocket mediate benzodiazepine efficacy and binding.
2011,
Pubmed
,
Xenbase
Morris,
Insight into the mechanism of action of neuroactive steroids.
2004,
Pubmed
,
Xenbase
Mowrey,
Asymmetric ligand binding facilitates conformational transitions in pentameric ligand-gated ion channels.
2013,
Pubmed
Murail,
Molecular mechanism for the dual alcohol modulation of Cys-loop receptors.
2012,
Pubmed
Nury,
One-microsecond molecular dynamics simulation of channel gating in a nicotinic receptor homologue.
2010,
Pubmed
Nury,
X-ray structures of general anaesthetics bound to a pentameric ligand-gated ion channel.
2011,
Pubmed
Parikh,
Structure of the M2 transmembrane segment of GLIC, a prokaryotic Cys loop receptor homologue from Gloeobacter violaceus, probed by substituted cysteine accessibility.
2011,
Pubmed
Pedretti,
VEGA--an open platform to develop chemo-bio-informatics applications, using plug-in architecture and script programming.
2004,
Pubmed
Prevost,
A locally closed conformation of a bacterial pentameric proton-gated ion channel.
2012,
Pubmed
Sancar,
Allosteric modulators induce distinct movements at the GABA-binding site interface of the GABA-A receptor.
2011,
Pubmed
,
Xenbase
Sauguet,
Structural basis for potentiation by alcohols and anaesthetics in a ligand-gated ion channel.
2013,
Pubmed
Spurny,
Multisite binding of a general anesthetic to the prokaryotic pentameric Erwinia chrysanthemi ligand-gated ion channel (ELIC).
2013,
Pubmed
,
Xenbase
Swaminath,
Sequential binding of agonists to the beta2 adrenoceptor. Kinetic evidence for intermediate conformational states.
2004,
Pubmed
Swaminath,
Probing the beta2 adrenoceptor binding site with catechol reveals differences in binding and activation by agonists and partial agonists.
2005,
Pubmed
Trattnig,
Discovery of a novel allosteric modulator of 5-HT3 receptors: inhibition and potentiation of Cys-loop receptor signaling through a conserved transmembrane intersubunit site.
2012,
Pubmed
Trott,
AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading.
2010,
Pubmed
Unwin,
Refined structure of the nicotinic acetylcholine receptor at 4A resolution.
2005,
Pubmed
Venkatachalan,
Optimized expression vector for ion channel studies in Xenopus oocytes and mammalian cells using alfalfa mosaic virus.
2007,
Pubmed
,
Xenbase
Weng,
Anesthetic sensitivity of the Gloeobacter violaceus proton-gated ion channel.
2010,
Pubmed
,
Xenbase
Willenbring,
Isoflurane alters the structure and dynamics of GLIC.
2011,
Pubmed
Williams,
Structural evidence that propofol stabilizes different GABA(A) receptor states at potentiating and activating concentrations.
2002,
Pubmed
,
Xenbase
Ye,
Enhancement of glycine receptor function by ethanol is inversely correlated with molecular volume at position alpha267.
1998,
Pubmed
,
Xenbase
Zeller,
Inhibitory ligand-gated ion channels as substrates for general anesthetic actions.
2008,
Pubmed
Zhu,
Pore opening and closing of a pentameric ligand-gated ion channel.
2010,
Pubmed
Zhu,
Gating transition of pentameric ligand-gated ion channels.
2009,
Pubmed