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1.
Neuropsychopharmacology ; 36(11): 2244-57, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21716264

ABSTRACT

Nicotine prominently mediates the behavioral effects of tobacco consumption, either through smoking or when taking tobacco by snuff or chew. However, many studies question the exclusive role of nicotine in these effects. The use of preparations containing all the components of tobacco, such as tobacco and smoke extracts, may be more suitable than nicotine alone to investigate the behavioral effects of smoking and tobacco intake. In the present study, the electrophysiological effects of tobacco and smoke on ventral tegmental area dopaminergic (DA) neurons were examined in vivo in anesthetized wild-type (WT), ß2-nicotinic acetylcholine receptor (nAChR) knockout (ß2-/-), α4-/-, and α6-/- mice and compared with those of nicotine alone. In WT mice, smoke and nicotine had similar potentiating effects on DA cell activity, but the action of tobacco on neuronal firing was weak and often inhibitory. In particular, nicotine triggered strong bursting activity, whereas no bursting activity was observed after tobacco extract (ToE) administration. In ß2-/- mice, nicotine or extract elicited no modification of the firing patterns of DA cells, indicating that extract acts predominantly through nAChRs. The differences between DA cell activation profiles induced by tobacco and nicotine alone observed in WT persisted in α6-/- mice but not in α4-/- mice. These results would suggest that tobacco has lower addiction-generating properties compared with either nicotine alone or smoke. The weak activation and prominent inhibition obtained with ToEs suggest that tobacco contains compounds that counteract some of the activating effects of nicotine and promote inhibition on DA cell acting through α4ß2*-nAChRs. The nature of these compounds remains to be elucidated. It nevertheless confirms that nicotine is the main substance involved in the tobacco addiction-related activation of mesolimbic DA neurons.


Subject(s)
Action Potentials/drug effects , Dopaminergic Neurons/drug effects , Nicotiana , Nicotine/pharmacology , Plant Extracts/pharmacology , Smoke , Ventral Tegmental Area/drug effects , Action Potentials/physiology , Animals , Dopaminergic Neurons/physiology , Drug Synergism , HEK293 Cells , Humans , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Nicotine/metabolism , Plant Extracts/isolation & purification , Ventral Tegmental Area/physiology
2.
Nature ; 469(7330): 428-31, 2011 Jan 20.
Article in English | MEDLINE | ID: mdl-21248852

ABSTRACT

General anaesthetics have enjoyed long and widespread use but their molecular mechanism of action remains poorly understood. There is good evidence that their principal targets are pentameric ligand-gated ion channels (pLGICs) such as inhibitory GABA(A) (γ-aminobutyric acid) receptors and excitatory nicotinic acetylcholine receptors, which are respectively potentiated and inhibited by general anaesthetics. The bacterial homologue from Gloeobacter violaceus (GLIC), whose X-ray structure was recently solved, is also sensitive to clinical concentrations of general anaesthetics. Here we describe the crystal structures of the complexes propofol/GLIC and desflurane/GLIC. These reveal a common general-anaesthetic binding site, which pre-exists in the apo-structure in the upper part of the transmembrane domain of each protomer. Both molecules establish van der Waals interactions with the protein; propofol binds at the entrance of the cavity whereas the smaller, more flexible, desflurane binds deeper inside. Mutations of some amino acids lining the binding site profoundly alter the ionic response of GLIC to protons, and affect its general-anaesthetic pharmacology. Molecular dynamics simulations, performed on the wild type (WT) and two GLIC mutants, highlight differences in mobility of propofol in its binding site and help to explain these effects. These data provide a novel structural framework for the design of general anaesthetics and of allosteric modulators of brain pLGICs.


Subject(s)
Anesthetics, General/chemistry , Anesthetics, General/metabolism , Cyanobacteria/chemistry , Isoflurane/analogs & derivatives , Ligand-Gated Ion Channels/chemistry , Ligand-Gated Ion Channels/metabolism , Propofol/chemistry , Binding Sites/genetics , Crystallography, X-Ray , Desflurane , Electrophysiological Phenomena , Isoflurane/chemistry , Isoflurane/metabolism , Ligand-Gated Ion Channels/genetics , Ligands , Models, Molecular , Molecular Dynamics Simulation , Mutant Proteins/chemistry , Mutant Proteins/genetics , Mutant Proteins/metabolism , Propofol/metabolism , Protein Binding , Protein Structure, Tertiary , Protons
3.
J Physiol ; 588(Pt 4): 565-72, 2010 Feb 15.
Article in English | MEDLINE | ID: mdl-19995852

ABSTRACT

Pentameric ligand-gated ion channels (pLGICs) are widely expressed in the animal kingdom and are key players of neurotransmission by acetylcholine (ACh), gamma-amminobutyric acid (GABA), glycine and serotonin. It is now established that this family has a prokaryotic origin, since more than 20 homologues have been discovered in bacteria. In particular, the GLIC homologue displays a ligand-gated ion channel function and is activated by protons. The prokaryotic origin of these membrane proteins facilitated the X-ray structural resolution of the first members of this family. ELIC was solved at 3.3 A in a closed-pore conformation, and GLIC at up to 2.9 A in an apparently open-pore conformation. These data reveal many structural features, notably the architecture of the pore, including its gate and its selectivity filter, and the interactions between the protein and lipids. In addition, comparison of the structures of GLIC and ELIC hints at a mechanism of channel opening, which consists of both a quaternary twist and a tertiary deformation. This mechanism couples opening-closing motions of the channel with a global reorganization of the protein, including the subunit interface that holds the neurotransmitter binding sites in eukaryotic pLGICs.


Subject(s)
Bacterial Proteins/chemistry , Ion Channel Gating , Ion Channels/chemistry , Receptors, Neurotransmitter/chemistry , Amino Acid Sequence , Bacterial Proteins/physiology , Crystallography, X-Ray , Ion Channels/physiology , Molecular Sequence Data , Protein Structure, Quaternary , Protein Structure, Tertiary , Receptors, Neurotransmitter/physiology
4.
J Mol Neurosci ; 30(1-2): 63-4, 2006.
Article in English | MEDLINE | ID: mdl-17192629

ABSTRACT

Pentameric ligand-gated ion channels (LGICs) are fast-gating receptors, represented by cationic nicotinic acetylcholine (nAChR) and serotonin (5HT3R) receptors, and by anionic GABA and glycine (GlyR) receptors. Because of a highly conserved sequence of 13 amino acids flanked by two canonical cysteine residues shared by all members of the family, these receptors are also known as the Cys-loop family. These receptors are allosteric transmembrane proteins made of five identical (or not) subunits arranged (pseudo) symmetrically around a central ion pore in the membrane. In nAChR, upon ACh binding, the receptor interconverts into discrete allosteric states, with each state corresponding to a different physiological state: resting (closed), active (open), and desensitized (closed).


Subject(s)
Cysteine , Ion Channel Gating/physiology , Receptors, Nicotinic/physiology , Amino Acid Sequence , Binding Sites , Ligands , Mutant Chimeric Proteins/chemistry , Protein Structure, Tertiary , Protein Subunits/physiology , Receptors, Nicotinic/chemistry
5.
J Biol Chem ; 281(21): 14875-81, 2006 May 26.
Article in English | MEDLINE | ID: mdl-16527818

ABSTRACT

To learn about the mechanism of ion charge selectivity by invertebrate glutamate-gated chloride (GluCl) channels, we swapped segments between the GluClbeta receptor of Caenorhabditis elegans and the vertebrate cationic alpha7-acetylcholine receptor and monitored anionic/cationic permeability ratios. Complete conversion of the ion charge selectivity in a set of receptor microchimeras indicates that the selectivity filter of the GluClbeta receptor is created by a sequence connecting the first with the second transmembrane segments. A single substitution of a negatively charged residue within this sequence converted the selectivity of the GluClbeta receptor's pore from anionic to cationic. Unexpectedly, elimination of the charge of each basic residue of the selectivity filter, one at a time or concomitantly, moderately reduced the P(Cl)/P(Na) ratios, but the GluClbeta receptor's mutants retained high capacity to select Cl(-) over Na(+). These results indicate that, unlike the proposed case of anionic Gly- and gamma-aminobutyric acid-gated ion channels, positively charged residues do not play the key role in the selection of ionic charge by the GluClbeta receptor. Taken together with measurements of the effective open pore diameter and with structural modeling, the study presented here collectively indicates that in the most constricted part of the open GluClbeta receptor's channel, Cl(-) interacts with backbone amides, where it undergoes partial dehydration necessary for traversing the pore.


Subject(s)
Chloride Channels/chemistry , Chloride Channels/genetics , Chlorides/chemistry , Glutamates/chemistry , Mutation , Amino Acid Sequence , Animals , Caenorhabditis elegans , Electrophysiology , Humans , Models, Biological , Molecular Sequence Data , Recombinant Fusion Proteins/chemistry , Sequence Homology, Amino Acid
6.
Proc Natl Acad Sci U S A ; 102(50): 18207-12, 2005 Dec 13.
Article in English | MEDLINE | ID: mdl-16319224

ABSTRACT

Neurotransmitters such as acetylcholine (ACh) and glycine mediate fast synaptic neurotransmission by activating pentameric ligand-gated ion channels (LGICs). These receptors are allosteric transmembrane proteins that rapidly convert chemical messages into electrical signals. Neurotransmitters activate LGICs by interacting with an extracellular agonist-binding domain (ECD), triggering a tertiary/quaternary conformational change in the protein that results in the fast opening of an ion pore domain (IPD). However, the molecular mechanism that determines the fast opening of LGICs remains elusive. Here, we show by combining whole-cell and single-channel recordings of recombinant chimeras between the ECD of alpha7 nicotinic receptor (nAChR) and the IPD of the glycine receptor (GlyR) that only two GlyR amino acid residues of loop 7 (Cys-loop) from the ECD and at most five alpha7 nAChR amino acid residues of the M2-M3 loop (2-3L) from the IPD control the fast activation rates of the alpha7/Gly chimera and WT GlyR. Mutual interactions of these residues at a critical pivot point between the agonist-binding site and the ion channel fine-tune the intrinsic opening and closing rates of the receptor through stabilization of the transition state of activation. These data provide a structural basis for the fast opening of pentameric LGICs.


Subject(s)
Ion Channel Gating/physiology , Neurotransmitter Agents/metabolism , Receptors, Glycine/metabolism , Receptors, Nicotinic/metabolism , Acetylcholine/metabolism , Amino Acid Sequence , Animals , Bungarotoxins/metabolism , Cell Line , Chickens , Humans , Iodine Radioisotopes/metabolism , Kinetics , Models, Molecular , Molecular Sequence Data , Mutagenesis , Patch-Clamp Techniques , Protein Structure, Tertiary , Receptors, Glycine/genetics , Receptors, Nicotinic/genetics , alpha7 Nicotinic Acetylcholine Receptor
7.
Proc Natl Acad Sci U S A ; 102(44): 15877-82, 2005 Nov 01.
Article in English | MEDLINE | ID: mdl-16247006

ABSTRACT

Neurons regulate the propagation of chemoelectric signals throughout the nervous system by opening and closing ion channels, a process known as gating. Here, histidine-based metal-binding sites were engineered along the intrinsic pore of a chimeric Cys-loop receptor to probe state-dependent Zn(2+)-channel interactions. Patterns of Zn(2+) ion binding within the pore reveal that, in the closed state, the five pore-lining segments adopt an oblique orientation relative to the axis of ion conduction and constrict into a physical gate at their intracellular end. The interactions of Zn(2+) with the open state indicate that the five pore-lining segments should rigidly tilt to enable the movement of their intracellular ends away from the axis of ion conduction, so as to open the constriction (i.e., the gate). Alignment of the functional results with the 3D structure of an acetylcholine receptor allowed us to generate structural models accounting for the closed and open pore conformations and for a gating mechanism of a Cys-loop receptor.


Subject(s)
Ion Channel Gating , Ion Channels/chemistry , Ion Channels/physiology , Animals , Cell Line , Cell Membrane Permeability , Electrophysiology , Humans , Neurons/chemistry , Oocytes , Porosity , Protein Conformation , Protein Engineering , Receptors, Cholinergic/chemistry , Recombinant Fusion Proteins , Xenopus , Zinc/metabolism
8.
Proc Natl Acad Sci U S A ; 100(20): 11309-14, 2003 Sep 30.
Article in English | MEDLINE | ID: mdl-13679581

ABSTRACT

Nicotinic acetylcholine receptors (AChRs) belong to a superfamily of oligomeric proteins that transduce electric signals across the cell membrane on binding of neurotransmitters. These receptors harbor a large extracellular ligand-binding domain directly linked to an ion-conducting channel-forming domain that spans the cell membrane 20 times and considerably extends into the cytoplasm. Thus far, none of these receptor channels has been crystallized in three dimensions. The crystallization of the AChR from Torpedo marmorata electric organs is challenged here in lipidic-detergent matrices. Detergent-soluble AChR complexed with alpha-bungarotoxin (alphaBTx), a polypeptidic competitive antagonist, was purified. The AChR-alphaBTx complex was reconstituted in a lipidic matrix composed of monoolein bilayers that are structured in three dimensions. The alphaBTx was conjugated to a photo-stable fluorophore, enabling us to monitor the physical behavior of the receptor-toxin complex in the lipidic matrix under light stereomicroscope, and to freeze fracture regions containing the receptor-toxin complex for visualization under a transmission electron microscope. Conditions were established for forming 2D receptor-toxin lattices that are stacked in the third dimension. 3D AChR nanocrystals were thereby grown inside the highly viscous lipidic 3D matrix. Slow emulsification of the lipidic matrix converted these nanocrystals into 3D elongated thin crystal plates of micrometer size. The latter are stable in detergent-containing aqueous solutions and can currently be used for seeding and epitaxial growth, en route to crystals of appropriate dimensions for x-ray diffraction studies.


Subject(s)
Detergents/chemistry , Lipids/chemistry , Receptors, Cholinergic/ultrastructure , Animals , Bungarotoxins/chemistry , Crystallization , Microscopy, Electron , Receptors, Cholinergic/chemistry , Torpedo
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