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Regulatory Domains of GABAA Receptors

Dunne, Emma Louise; (2000) Regulatory Domains of GABAA Receptors. Doctoral thesis (Ph.D), UCL (University College London). Green open access

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GABAA receptors are the principal mediators of rapid, synaptic inhibition within the mammalian central nervous system. These receptors are hetero-oligomeric proteins that can be assembled from α(l-6), β(l-3), γ(l-3), δ &egr;, π and &thgr; subunit classes (Mehta & Ticku, 1999; Bonnert et al , 1999). Each subunit comprises a putative extracellular N- terminus, four putative transmembrane domains (TM), a large intracellular domain linking TM3 and TM4, and an extracellular C-terminus. The present study investigated these domains to identify molecular determinants affecting modulation of GABA A receptor function. An N-terminal histidine (H107) was implicated in mediating lower affinity Zn2+ binding on the ?3 subunit and also a possible role in homomeric receptor assembly/protein folding. Interestingly, mutation of the aligned residue on the α1 subunit (H109) strongly influenced GABA but not Zn2+ potency. Substitution of α1H141 located in the cysteine loop region of the N-terminal domain reduced Zn 2+ sensitivity of heteromeric GABAA receptors. An electrophysiological approach based on the relative insensitivity to Zn2+ generated by a TM2 mutation (H267A) was used to predict a tetrameric stoichiometry for β3 subunit homomeric GABAA receptors. In addition, the substituted histidine accessibility method (SHAM) was developed to probe TM2 by individually substituting putative channel lining residues with histidines in homomeric β3 H267A GABAA receptors. It was inferred that Zn2+ is able to penetrate the anion channel at least as far as residue 263. Finally, an initial investigation of residues in the large intracellular TM3-TM4 domain responsible for tyrosine phosphorylation of α1β1γ2S receptors discovered that external application of protein tyrosine kinase (PTK) inhibitors directly modulate GABAA receptors independently of tyrosine kinases. The present study into regulatory domains of the GABAA receptor revealed important novel N-terminal residues for Zn2+ inhibition and a novel non-specific interaction of PTK inhibitors with the GABA A receptor. In addition, a method for probing ion channel properties using histidine was devised and the stoichiometry of a GABAA receptor complex was predicted using the binomial theorem.

Type: Thesis (Doctoral)
Qualification: Ph.D
Title: Regulatory Domains of GABAA Receptors
Open access status: An open access version is available from UCL Discovery
Language: English
Additional information: Thesis digitised by ProQuest.
URI: https://discovery.ucl.ac.uk/id/eprint/10111214
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