Subunit arrangement of γ-aminobutyric acid type a receptors

被引:183
作者
Baumann, SW [1 ]
Baur, R [1 ]
Sigel, E [1 ]
机构
[1] Univ Bern, Dept Pharmacol, CH-3010 Bern, Switzerland
关键词
D O I
10.1074/jbc.M105240200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The GABA(A) receptors are ligand-gated chloride channels. The subunit stoichiometry of the receptors is controversial; four, five, or six subunits per receptor molecule have been proposed for alpha beta receptors, whereas alpha beta gamma receptors are assumed to be pentamers. In this study, alpha-beta and beta-alpha tandem cDNAs from the alpha1 and beta2 subunits of the GABA(A) receptor were constructed. We determined the minimal length of the linker that is required between the two subunits for functional channel expression for each of the tandem constructs. 10- and 23-amino acid residues are required for alpha-beta and beta-alpha, respectively. The tandem constructs either alone or in combination with each other failed to express functional channels in Xenopus oocytes. Therefore, we can exclude tetrameric or hexameric alpha beta GABA(A) receptors. We can also exclude proteolysis of the tandem constructs. In addition, the tandem constructs were combined with single alpha, beta, or gamma subunits to allow formation of pentameric arrangements. In contrast to the combination with alpha subunits, the combination with either beta or gamma subunits led to expression of functional channels. Therefore, a pentameric arrangement containing two alpha1 and three beta2 subunits is proposed for the receptor composed of alpha and beta subunits. Our findings also favor an arrangement beta alpha gamma beta alpha for the receptor composed of alpha, beta, and gamma subunits.
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收藏
页码:36275 / 36280
页数:6
相关论文
共 40 条
[1]  
ANGELOTTI TP, 1993, J NEUROSCI, V13, P1429
[2]  
ANGELOTTI TP, 1993, J NEUROSCI, V13, P1418
[3]   STOICHIOMETRY OF A RECOMBINANT GABA(A) RECEPTOR DEDUCED FROM MUTATION-INDUCED RECTIFICATION [J].
BACKUS, KH ;
ARIGONI, M ;
DRESCHER, U ;
SCHEURER, L ;
MALHERBE, P ;
MOHLER, H ;
BENSON, JA .
NEUROREPORT, 1993, 5 (03) :285-288
[4]  
BENKE D, 1994, J BIOL CHEM, V269, P27100
[5]  
Chang YC, 1996, J NEUROSCI, V16, P5415
[6]   Assembly and cell surface expression of heteromeric and homomeric gamma-aminobutyric acid type A receptors [J].
Connolly, CN ;
Krishek, BJ ;
McDonald, BJ ;
Smart, TG ;
Moss, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (01) :89-96
[7]   Insensitivity to anaesthetic agents conferred by a class of GABA(A) receptor subunit [J].
Davies, PA ;
Hanna, MC ;
Hales, TG ;
Kirkness, EF .
NATURE, 1997, 385 (6619) :820-823
[8]   FUNCTIONAL AND MOLECULAR DISTINCTION BETWEEN RECOMBINANT RAT GABA-A RECEPTOR SUBTYPES BY ZN-2+ [J].
DRAGUHN, A ;
VERDORN, TA ;
EWERT, M ;
SEEBURG, PH ;
SAKMANN, B .
NEURON, 1990, 5 (06) :781-788
[9]   SUBUNIT SELECTIVITY AND EPITOPE CHARACTERIZATION OF MABS DIRECTED AGAINST THE GABA-A BENZODIAZEPINE RECEPTOR [J].
EWERT, M ;
SHIVERS, BD ;
LUDDENS, H ;
MOHLER, H ;
SEEBURG, PH .
JOURNAL OF CELL BIOLOGY, 1990, 110 (06) :2043-2048
[10]  
Gorrie GH, 1997, J NEUROSCI, V17, P6587