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Protein Sci
2009 Nov 01;1811:2371-83. doi: 10.1002/pro.247.
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Structural model of rho1 GABAC receptor based on evolutionary analysis: Testing of predicted protein-protein interactions involved in receptor assembly and function.
Adamian L
,
Gussin HA
,
Tseng YY
,
Muni NJ
,
Feng F
,
Qian H
,
Pepperberg DR
,
Liang J
.
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The homopentameric rho1 GABA(C) receptor is a ligand-gated ion channel with a binding pocket for gamma-aminobutyric acid (GABA) at the interfaces of N-terminal extracellular domains. We combined evolutionary analysis, structural modeling, and experimental testing to study determinants of GABA(C) receptor assembly and channel gating. We estimated the posterior probability of selection pressure at amino acid residue sites measured as omega-values and built a comparative structural model, which identified several polar residues under strong selection pressure at the subunit interfaces that may form intersubunit hydrogen bonds or salt bridges. At three selected sites (R111, T151, and E55), mutations disrupting intersubunit interactions had strong effects on receptor folding, assembly, and function. We next examined the role of a predicted intersubunit salt bridge for residue pair R158-D204. The mutant R158D, where the positively charged residue is replaced by a negatively charged aspartate, yielded a partially degraded receptor and lacked membrane surface expression. The membrane surface expression was rescued by the double mutant R158D-D204R, where positive and negative charges are switched, although the mutant receptor was inactive. The single mutants R158A, D204R, and D204A exhibited diminished activities and altered kinetic profiles with fast recovery kinetics, suggesting that R158-D204 salt bridge perhaps stabilizes the open state of the GABA(C) receptor. Our results emphasize the functional importance of highly conserved polar residues at the protein-protein interfaces in GABA(C) rho1 receptors and demonstrate how the integration of computational and experimental approaches can aid discovery of functionally important interactions.
Abdel-Halim,
A molecular basis for agonist and antagonist actions at GABA(C) receptors.
2008, Pubmed
Abdel-Halim,
A molecular basis for agonist and antagonist actions at GABA(C) receptors.
2008,
Pubmed
Amin,
Homomeric rho 1 GABA channels: activation properties and domains.
1994,
Pubmed
,
Xenbase
Bocquet,
X-ray structure of a pentameric ligand-gated ion channel in an apparently open conformation.
2009,
Pubmed
Bourne,
Crystal structure of a Cbtx-AChBP complex reveals essential interactions between snake alpha-neurotoxins and nicotinic receptors.
2005,
Pubmed
Brejc,
Crystal structure of an ACh-binding protein reveals the ligand-binding domain of nicotinic receptors.
2001,
Pubmed
Caffrey,
PFAAT version 2.0: a tool for editing, annotating, and analyzing multiple sequence alignments.
2007,
Pubmed
Carland,
Charged residues at the 2' position of human GABAC rho 1 receptors invert ion selectivity and influence open state probability.
2004,
Pubmed
Celie,
Crystal structure of acetylcholine-binding protein from Bulinus truncatus reveals the conserved structural scaffold and sites of variation in nicotinic acetylcholine receptors.
2005,
Pubmed
Celie,
Nicotine and carbamylcholine binding to nicotinic acetylcholine receptors as studied in AChBP crystal structures.
2004,
Pubmed
Chebib,
GABAC receptor ion channels.
2004,
Pubmed
Cole,
The Jpred 3 secondary structure prediction server.
2008,
Pubmed
Corringer,
Nicotinic receptors at the amino acid level.
2000,
Pubmed
Cromer,
Anxiety over GABA(A) receptor structure relieved by AChBP.
2002,
Pubmed
Dellisanti,
Crystal structure of the extracellular domain of nAChR alpha1 bound to alpha-bungarotoxin at 1.94 A resolution.
2007,
Pubmed
Edelsbrunner,
On the definition and the construction of pockets in macromolecules.
1996,
Pubmed
Hansen,
Structures of Aplysia AChBP complexes with nicotinic agonists and antagonists reveal distinctive binding interfaces and conformations.
2005,
Pubmed
Harrison,
Molecular modeling of the GABA(C) receptor ligand-binding domain.
2006,
Pubmed
Harrison,
Locating the carboxylate group of GABA in the homomeric rho GABA(A) receptor ligand-binding pocket.
2006,
Pubmed
Henchman,
Asymmetric structural motions of the homomeric alpha7 nicotinic receptor ligand binding domain revealed by molecular dynamics simulation.
2003,
Pubmed
Hilf,
Structure of a potentially open state of a proton-activated pentameric ligand-gated ion channel.
2009,
Pubmed
Johnston,
GABAc receptors: relatively simple transmitter -gated ion channels?
1996,
Pubmed
Karlin,
Toward a structural basis for the function of nicotinic acetylcholine receptors and their cousins.
1995,
Pubmed
Kusama,
Mutagenesis of the GABA rho 1 receptor alters agonist affinity and channel gating.
1994,
Pubmed
,
Xenbase
Larkin,
Clustal W and Clustal X version 2.0.
2007,
Pubmed
Lecompte,
Multiple alignment of complete sequences (MACS) in the post-genomic era.
2001,
Pubmed
Liang,
Analytical shape computation of macromolecules: II. Inaccessible cavities in proteins.
1998,
Pubmed
Nei,
Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions.
1986,
Pubmed
Osolodkin,
Molecular modeling of ligand-receptor interactions in GABA C receptor.
2009,
Pubmed
Qian,
A comparison of GABAC and rho subunit receptors from the white perch retina.
1997,
Pubmed
,
Xenbase
Reeves,
The molecular basis of the structure and function of the 5-HT3 receptor: a model ligand-gated ion channel (review).
2002,
Pubmed
Rose,
Hydrophobicity of amino acid residues in globular proteins.
1985,
Pubmed
Sali,
Comparative protein modelling by satisfaction of spatial restraints.
1993,
Pubmed
Sarto-Jackson,
Identification of amino acid residues important for assembly of GABA receptor alpha1 and gamma2 subunits.
2006,
Pubmed
Sedelnikova,
Mapping the rho1 GABA(C) receptor agonist binding pocket. Constructing a complete model.
2005,
Pubmed
Sine,
Recent advances in Cys-loop receptor structure and function.
2006,
Pubmed
Smit,
A glia-derived acetylcholine-binding protein that modulates synaptic transmission.
2001,
Pubmed
Speranskiy,
Homology modeling and molecular dynamics simulations of the glycine receptor ligand binding domain.
2007,
Pubmed
Tasneem,
Identification of the prokaryotic ligand-gated ion channels and their implications for the mechanisms and origins of animal Cys-loop ion channels.
2005,
Pubmed
Thompson,
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.
1994,
Pubmed
Torres,
Identification of a tyrosine in the agonist binding site of the homomeric rho1 gamma-aminobutyric acid (GABA) receptor that, when mutated, produces spontaneous opening.
2002,
Pubmed
,
Xenbase
Tseng,
Are residues in a protein folding nucleus evolutionarily conserved?
2004,
Pubmed
Tseng,
Estimation of amino acid residue substitution rates at local spatial regions and application in protein function inference: a Bayesian Monte Carlo approach.
2006,
Pubmed
Unwin,
Refined structure of the nicotinic acetylcholine receptor at 4A resolution.
2005,
Pubmed
Vu,
Activation of membrane receptors by a neurotransmitter conjugate designed for surface attachment.
2005,
Pubmed
,
Xenbase
Wang,
Establishing an ion pair interaction in the homomeric rho1 gamma-aminobutyric acid type A receptor that contributes to the gating pathway.
2007,
Pubmed
,
Xenbase
Wible,
Cloning and expression of a novel K+ channel regulatory protein, KChAP.
1998,
Pubmed
,
Xenbase
Yang,
PAML 4: phylogenetic analysis by maximum likelihood.
2007,
Pubmed
Yang,
PAML: a program package for phylogenetic analysis by maximum likelihood.
1997,
Pubmed
Yang,
Maximum-likelihood estimation of phylogeny from DNA sequences when substitution rates differ over sites.
1993,
Pubmed
Zhang,
Structural determinants for antagonist pharmacology that distinguish the rho1 GABAC receptor from GABAA receptors.
2008,
Pubmed
,
Xenbase
Zhang,
Agonist- and antagonist-induced conformational changes of loop F and their contributions to the rho1 GABA receptor function.
2009,
Pubmed
,
Xenbase
Zhang,
Structure and function of GABA(C) receptors: a comparison of native versus recombinant receptors.
2001,
Pubmed