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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
13
pubmed:dateCreated
2006-3-29
pubmed:abstractText
Several major insecticides, including alpha-endosulfan, lindane, and fipronil, and the botanical picrotoxinin are noncompetitive antagonists (NCAs) for the GABA receptor. We showed earlier that human beta(3) homopentameric GABA(A) receptor recognizes all of the important GABAergic insecticides and reproduces the high insecticide sensitivity and structure-activity relationships of the native insect receptor. Despite large structural diversity, the NCAs are proposed to fit a single binding site in the chloride channel lumen lined by five transmembrane 2 segments. This hypothesis is examined with the beta(3) homopentamer by mutagenesis, pore structure studies, NCA binding, and molecular modeling. The 15 amino acids in the cytoplasmic half of the pore were mutated to cysteine, serine, or other residue for 22 mutants overall. Localization of A-1'C, A2'C, T6'C, and L9'C (index numbers for the transmembrane 2 region) in the channel lumen was established by disulfide cross-linking. Binding of two NCA radioligands [(3)H]1-(4-ethynylphenyl)-4-n-propyl-2,6,7-trioxabicyclo[2.2.2]octane and [(3)H] 3,3-bis-trifluoromethyl-bicyclo[2,2,1]heptane-2,2-dicarbonitrile was dramatically reduced with 8 of the 15 mutated positions, focusing attention on A2', T6', and L9' as proposed binding sites, consistent with earlier mutagenesis studies. The cytoplasmic half of the beta3 homopentamer pore was modeled as an alpha-helix. The six NCAs listed above plus t-butylbicyclophosphorothionate fit the 2' to 9' pore region forming hydrogen bonds with the T6' hydroxyl and hydrophobic interactions with A2', T6', and L9' alkyl substituents, thereby blocking the channel. Thus, widely diverse NCA structures fit the same GABA receptor beta subunit site with important implications for insecticide cross-resistance and selective toxicity between insects and mammals.
pubmed:commentsCorrections
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pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
28
pubmed:volume
103
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5185-90
pubmed:dateRevised
2010-9-16
pubmed:meshHeading
pubmed-meshheading:16537435-Amino Acid Sequence, pubmed-meshheading:16537435-Animals, pubmed-meshheading:16537435-Bicyclo Compounds, pubmed-meshheading:16537435-Bicyclo Compounds, Heterocyclic, pubmed-meshheading:16537435-Binding Sites, pubmed-meshheading:16537435-Cell Line, pubmed-meshheading:16537435-Drosophila, pubmed-meshheading:16537435-GABA Antagonists, pubmed-meshheading:16537435-Gene Expression, pubmed-meshheading:16537435-Humans, pubmed-meshheading:16537435-Models, Molecular, pubmed-meshheading:16537435-Molecular Sequence Data, pubmed-meshheading:16537435-Mutation, pubmed-meshheading:16537435-Nitriles, pubmed-meshheading:16537435-Protein Binding, pubmed-meshheading:16537435-Protein Structure, Quaternary, pubmed-meshheading:16537435-Protein Subunits, pubmed-meshheading:16537435-Rats, pubmed-meshheading:16537435-Receptors, GABA, pubmed-meshheading:16537435-Sequence Alignment, pubmed-meshheading:16537435-Structure-Activity Relationship
pubmed:year
2006
pubmed:articleTitle
Structural model for gamma-aminobutyric acid receptor noncompetitive antagonist binding: widely diverse structures fit the same site.
pubmed:affiliation
Environmental Chemistry and Toxicology Laboratory, Department of Environmental Science, Policy, and Management, College of Chemistry, University of California, Berkeley, CA 94720, USA.
pubmed:publicationType
Journal Article
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