Impact of subunit positioning on GABAA receptor function

被引:34
作者
Sigel, E. [1 ]
Baur, R.
Boulineau, N.
Minier, F.
机构
[1] Univ Bern, Dept Biochem & Mol Med, CH-3012 Bern, Switzerland
[2] Med Univ Ohio, Dept Neurol, Toledo, OH 43614 USA
[3] Inst Francois Magendie, Equipe INSERM, AVENIR 3, IFR8, F-33000 Bordeaux, France
关键词
benzodiazepine; concatenated subunit; gamma-aminobutyric acid (GABA); gamma-aminobutyric acid type A receptor (GABA(A) receptor); subunit positioning; subunit specificity;
D O I
10.1042/BST0340868
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 major isoforms of the GABA(A) (gamma-aminobutyric acid type A) receptor are composed of two of, two and one gamma subunit. Thus alpha and beta subunits occur twice in the receptor pentamer. As it is well documented that different isoforms of alpha and beta subunits can co-exist in the same pentamer, the question is raised whether the relative position of a subunit isoform affects the functional properties of the receptor. We have used subunit concatenation to engineer receptors of well-defined subunit arrangement to study this question. Although all five subunits may be concatenated, we have focused on the combination of triple and dual subunit constructs. We review here what is known so far on receptors containing simultaneously alpha(1) and alpha(6) subunits and receptors containing beta(1) and beta(2) subunits. Subunit concatenation may not only be used to study receptors containing two different subunit isoforms, but also to introduce a point mutation into a defined position in receptors containing either two alpha or beta subunits, or to study the receptor architecture of receptors containing unconventional GABAA receptor subunits. Similar approaches may be used to characterize other members of the pentameric ligand-gated ion channel family, including nicotinic acetylcholine receptors, glycine receptors and 5-HT3 (5-hydroxytryptamine) receptors.
引用
收藏
页码:868 / 871
页数:4
相关论文
共 24 条
[1]   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
[2]  
Barnard EA, 1998, PHARMACOL REV, V50, P291
[3]  
Baumann SW, 2003, J NEUROSCI, V23, P11158
[4]   Forced subunit assembly in α1β2γ2 GABAA receptors -: Insight into the absolute arrangement [J].
Baumann, SW ;
Baur, R ;
Sigel, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (48) :46020-46025
[5]   Subunit arrangement of γ-aminobutyric acid type a receptors [J].
Baumann, SW ;
Baur, R ;
Sigel, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (39) :36275-36280
[6]   A GABAA receptor of defined subunit composition and positioning:: Concatenation of five subunits [J].
Baur, R ;
Minier, F ;
Sigel, E .
FEBS LETTERS, 2006, 580 (06) :1616-1620
[7]   Benzodiazepines affect channel opening of GABAA receptors induced by either agonist binding site [J].
Baur, R ;
Sigel, E .
MOLECULAR PHARMACOLOGY, 2005, 67 (04) :1005-1008
[8]   Tandem subunits effectively constrain GABAA receptor stoichiometry and recapitulate receptor kinetics but are insensitive to GABAA receptor-associated protein [J].
Boileau, AJ ;
Pearce, RA ;
Czajkowski, C .
JOURNAL OF NEUROSCIENCE, 2005, 25 (49) :11219-11230
[9]   The relative amount of cRNA coding for γ2 subunits affects stimulation by benzodiazepines in GABAA receptors expressed in Xenopus oocytes [J].
Boileau, AJ ;
Baur, R ;
Sharkey, LM ;
Sigel, E ;
Czajkowski, C .
NEUROPHARMACOLOGY, 2002, 43 (04) :695-700
[10]   Consequence of the presence of two different β subunit isoforms in a GABAA receptor [J].
Boulineau, N ;
Baur, R ;
Minier, F ;
Sigel, E .
JOURNAL OF NEUROCHEMISTRY, 2005, 95 (06) :1724-1731