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Neurotoxins from snake venoms and α-conotoxin ImI inhibit functionally active ionotropic γ-aminobutyric acid (GABA) receptors.
Kudryavtsev DS
,
Shelukhina IV
,
Son LV
,
Ojomoko LO
,
Kryukova EV
,
Lyukmanova EN
,
Zhmak MN
,
Dolgikh DA
,
Ivanov IA
,
Kasheverov IE
,
Starkov VG
,
Ramerstorfer J
,
Sieghart W
,
Tsetlin VI
,
Utkin YN
.
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Ionotropic receptors of γ-aminobutyric acid (GABAAR) regulate neuronal inhibition and are targeted by benzodiazepines and general anesthetics. We show that a fluorescent derivative of α-cobratoxin (α-Ctx), belonging to the family of three-finger toxins from snake venoms, specifically stained the α1β3γ2 receptor; and at 10 μm α-Ctx completely blocked GABA-induced currents in this receptor expressed in Xenopus oocytes (IC50 = 236 nm) and less potently inhibited α1β2γ2 ≈ α2β2γ2 > α5β2γ2 > α2β3γ2 and α1β3δ GABAARs. The α1β3γ2 receptor was also inhibited by some other three-finger toxins, long α-neurotoxin Ls III and nonconventional toxin WTX. α-Conotoxin ImI displayed inhibitory activity as well. Electrophysiology experiments showed mixed competitive and noncompetitive α-Ctx action. Fluorescent α-Ctx, however, could be displaced by muscimol indicating that most of the α-Ctx-binding sites overlap with the orthosteric sites at the β/α subunit interface. Modeling and molecular dynamic studies indicated that α-Ctx or α-bungarotoxin seem to interact with GABAAR in a way similar to their interaction with the acetylcholine-binding protein or the ligand-binding domain of nicotinic receptors. This was supported by mutagenesis studies and experiments with α-conotoxin ImI and a chimeric Naja oxiana α-neurotoxin indicating that the major role in α-Ctx binding to GABAAR is played by the tip of its central loop II accommodating under loop C of the receptors.
Alfonso,
Diazepam binding inhibitor promotes progenitor proliferation in the postnatal SVZ by reducing GABA signaling.
2012, Pubmed
Alfonso,
Diazepam binding inhibitor promotes progenitor proliferation in the postnatal SVZ by reducing GABA signaling.
2012,
Pubmed
Antil-Delbeke,
Molecular determinants by which a long chain toxin from snake venom interacts with the neuronal alpha 7-nicotinic acetylcholine receptor.
2000,
Pubmed
Ashton,
The diagnosis and management of benzodiazepine dependence.
2005,
Pubmed
Berg,
Binding of -bungarotoxin to acetylcholine receptors in mammalian muscle (snake venom-denervated muscle-neonatal muscle-rat diaphragm-SDS-polyacrylamide gel electrophoresis).
1972,
Pubmed
Bergmann,
A unified model of the GABA(A) receptor comprising agonist and benzodiazepine binding sites.
2013,
Pubmed
Bogdanov,
Synaptic GABAA receptors are directly recruited from their extrasynaptic counterparts.
2006,
Pubmed
Bourne,
Crystal structure of a Cbtx-AChBP complex reveals essential interactions between snake alpha-neurotoxins and nicotinic receptors.
2005,
Pubmed
Christian,
Endogenous positive allosteric modulation of GABA(A) receptors by diazepam binding inhibitor.
2013,
Pubmed
Clarke,
Nicotinic binding in rat brain: autoradiographic comparison of [3H]acetylcholine, [3H]nicotine, and [125I]-alpha-bungarotoxin.
1985,
Pubmed
Dellisanti,
Crystal structure of the extracellular domain of nAChR alpha1 bound to alpha-bungarotoxin at 1.94 A resolution.
2007,
Pubmed
Dubovskii,
Cobra cardiotoxins: membrane interactions and pharmacological potential.
2014,
Pubmed
Eastman,
OpenMM: A Hardware Independent Framework for Molecular Simulations.
2015,
Pubmed
Gergalova,
Mitochondria express α7 nicotinic acetylcholine receptors to regulate Ca2+ accumulation and cytochrome c release: study on isolated mitochondria.
2012,
Pubmed
Grishin,
Amino acid sequence of neurotoxin I from Naja naja oxiana venom.
1974,
Pubmed
Guex,
Automated comparative protein structure modeling with SWISS-MODEL and Swiss-PdbViewer: a historical perspective.
2009,
Pubmed
Hannan,
Snake neurotoxin α-bungarotoxin is an antagonist at native GABA(A) receptors.
2015,
Pubmed
Hansen,
Structural and ligand recognition characteristics of an acetylcholine-binding protein from Aplysia californica.
2004,
Pubmed
Humphrey,
VMD: visual molecular dynamics.
1996,
Pubmed
Joshi,
GABAA receptor membrane insertion rates are specified by their subunit composition.
2013,
Pubmed
Kasheverov,
Naturally occurring and synthetic peptides acting on nicotinic acetylcholine receptors.
2009,
Pubmed
Krishek,
Homomeric beta 1 gamma-aminobutyric acid A receptor-ion channels: evaluation of pharmacological and physiological properties.
1996,
Pubmed
,
Xenbase
Lyukmanova,
Bacterial expression, NMR, and electrophysiology analysis of chimeric short/long-chain alpha-neurotoxins acting on neuronal nicotinic receptors.
2007,
Pubmed
,
Xenbase
Maslennikov,
NMR spatial structure of alpha-conotoxin ImI reveals a common scaffold in snail and snake toxins recognizing neuronal nicotinic acetylcholine receptors.
1999,
Pubmed
McCann,
The cholinergic antagonist alpha-bungarotoxin also binds and blocks a subset of GABA receptors.
2006,
Pubmed
,
Xenbase
Miller,
Crystal structure of a human GABAA receptor.
2014,
Pubmed
Mirheydari,
Unexpected Properties of δ-Containing GABAA Receptors in Response to Ligands Interacting with the α+ β- Site.
2014,
Pubmed
,
Xenbase
Mordvintsev,
Weak toxin WTX from Naja kaouthia cobra venom interacts with both nicotinic and muscarinic acetylcholine receptors.
2009,
Pubmed
Olsen,
Picrotoxin-like channel blockers of GABAA receptors.
2006,
Pubmed
Osipov,
Dimeric α-cobratoxin X-ray structure: localization of intermolecular disulfides and possible mode of binding to nicotinic acetylcholine receptors.
2012,
Pubmed
Pettersen,
UCSF Chimera--a visualization system for exploratory research and analysis.
2004,
Pubmed
Razet,
Use of bicuculline, a GABA antagonist, as a template for the development of a new class of ligands showing positive allosteric modulation of the GABA(A) receptor.
2000,
Pubmed
,
Xenbase
Rosso,
MmTX1 and MmTX2 from coral snake venom potently modulate GABAA receptor activity.
2015,
Pubmed
,
Xenbase
Shelukhina,
Presence of alpha7 nicotinic acetylcholine receptors on dorsal root ganglion neurons proved using knockout mice and selective alpha-neurotoxins in histochemistry.
2009,
Pubmed
Sieghart,
Allosteric modulation of GABAA receptors via multiple drug-binding sites.
2015,
Pubmed
Sigel,
Structure, function, and modulation of GABA(A) receptors.
2012,
Pubmed
Starkov,
[New weak toxins from the cobra venom].
2009,
Pubmed
Tsetlin,
Detection of alpha7 nicotinic acetylcholine receptors with the aid of antibodies and toxins.
2007,
Pubmed
Tsetlin,
EPR and fluorescence study of interaction of Naja naja oxiana neurotoxin II and its derivatives with acetylcholine receptor protein from Torpedo marmorata.
1979,
Pubmed
Utkin,
Labeling of Torpedo californica nicotinic acetylcholine receptor subunits by cobratoxin derivatives with photoactivatable groups of different chemical nature at Lys23.
1998,
Pubmed
Utkin,
"Weak toxin" from Naja kaouthia is a nontoxic antagonist of alpha 7 and muscle-type nicotinic acetylcholine receptors.
2001,
Pubmed
,
Xenbase
Wyrembek,
Inhibitory effects of oenanthotoxin analogues on GABAergic currents in cultured rat hippocampal neurons depend on the polyacetylenes' polarity.
2012,
Pubmed
Zhang,
Alpha-cobratoxin inhibits T-type calcium currents through muscarinic M4 receptor and Gο-protein βγ subunits-dependent protein kinase A pathway in dorsal root ganglion neurons.
2012,
Pubmed
Zouridakis,
Crystal structures of free and antagonist-bound states of human α9 nicotinic receptor extracellular domain.
2014,
Pubmed
,
Xenbase