https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=pubmed&id=19156871&retmode=xml&tool=Litmetric&email=readroberts32@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09 191568712009073020101118
1097-45478782009JunJournal of neuroscience researchJ Neurosci ResDistinct properties of murine alpha 5 gamma-aminobutyric acid type a receptors revealed by biochemical fractionation and mass spectroscopy.173717471737-4710.1002/jnr.21991Gamma-aminobutyric acid type A receptors (GABA(A)Rs) that contain the alpha 5 subunit are expressed predominantly in the hippocampus, where they regulate learning and memory processes. Unlike conventional postsynaptic receptors, GABA(A)Rs containing the alpha 5 subunit (alpha 5 GABA(A)Rs) are localized primarily to extrasynaptic regions of neurons, where they generate a tonic inhibitory conductance. The unique characteristics of alpha 5 GABA(A)Rs have been examined with pharmacological, immunostaining, and electrophysiological techniques; however, little is known about their biochemical properties. The aim of this study was to modify existing purification and enrichment techniques to isolate alpha 5 GABA(A)Rs preferentially from the mouse hippocampus and to identify the alpha 5 subunit by using tandem mass spectroscopy (MS/MS). The results showed that the detergent solubility of the alpha 5 subunits was distinct from that of alpha1 and alpha2 subunits, and the relative distribution of the alpha 5 subunits in Triton X-100-soluble fractions was correlated with that of the extracellular protein radixin but not with that of the postsynaptic protein gephyrin. Mass spectrometry identified the alpha 5 subunit and showed that this subunit associates with multiple alpha, beta, and gamma subunits, but most frequently the beta 3 subunit. Thus, the alpha 5 subunits coassemble with similar subunits as their synaptic counterparts yet have a distinct detergent solubility profile. Mass spectroscopy now offers a method for detecting and characterizing factors that confer the unique detergent solubility and possibly cellular location of alpha 5 GABA(A)Rs in hippocampal neurons.(c) 2009 Wiley-Liss, Inc.JuYoung HYHDepartment of Physiology, University of Toronto, Toronto, Ontario, Canada.GuzzoAngelinaAChiuMary WMWTaylorPaulPMoranMichael FMFGurdJames WJWMacDonaldJohn FJFOrserBeverley ABAengJournal ArticleResearch Support, Non-U.S. Gov't
United StatesJ Neurosci Res76001110360-40120Cytoskeletal Proteins0Gabra5 protein, mouse0Gabrb3 protein, mouse0Membrane Proteins0Protein Subunits0Receptors, GABA-A144517-21-5radixin56-12-2gamma-Aminobutyric AcidIMAnimalsChemical FractionationmethodsCytoskeletal ProteinsmetabolismExtracellular SpacemetabolismHippocampusmetabolismultrastructureMass SpectrometrymethodsMembrane ProteinsmetabolismMiceMice, Inbred C57BLMice, KnockoutNeural InhibitionphysiologyNeurochemistrymethodsNeuronsmetabolismultrastructureProtein Structure, TertiaryphysiologyProtein SubunitschemistrymetabolismProteomicsmethodsReceptors, GABA-AchemistrymetabolismphysiologySolubilitySynaptic MembranesmetabolismultrastructureSynaptic Transmissionphysiologygamma-Aminobutyric Acidmetabolism
200912290200912290200973190ppublish1915687110.1002/jnr.21991