Assembly of GABAA receptors (Review)

被引:37
|
作者
Sarto-Jackson, Isabella [1 ]
Sieghart, Werner [1 ]
机构
[1] Med Univ Vienna, Ctr Brain Res, Div Biochem & Mol Biol, A-1090 Vienna, Austria
基金
奥地利科学基金会;
关键词
GABA(A) receptor; heterogeneity; assembly; intermediates; mechanism;
D O I
10.1080/09687680801914516
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
GABA(A) receptors are the major inhibitory transmitter receptors in the central nervous system. They are chloride ion channels that can be opened by -aminobutyric acid (GABA) and are the targets of action of a variety of pharmacologically and clinically important drugs. GABA(A) receptors are composed of five subunits that can belong to different subunit classes. The existence of 19 different subunits gives rise to the formation of a large variety of distinct GABA(A) receptor subtypes in the brain. The majority of GABA(A) receptors seems to be composed of two , two and one subunit and the occurrence of a defined subunit stoichiometry and arrangement in receptors strongly indicates that assembly of GABA(A) receptors proceeds via defined pathways. Based on the differential ability of subunits to interact with each other, a variety of studies have been performed to identify amino acid sequences or residues important for assembly. Such residues might be involved in direct protein-protein interactions, or in stabilizing direct contact sites in other regions of the subunit. Several homo-oligomeric or hetero-oligomeric assembly intermediates could be the starting point of GABA(A) receptor assembly but so far no unequivocal assembly mechanism has been identified. Possible mechanisms of assembly of GABA(A) receptors are discussed in the light of recent publications.
引用
收藏
页码:302 / 310
页数:9
相关论文
共 50 条
  • [1] Assembly and intracellular trafficking of GABAA receptors
    Barnes, EM
    INTERNATIONAL REVIEW OF NEUROBIOLOGY, VOL 48, 2001, 48 : 1 - 29
  • [2] Trafficking and potential assembly patterns of ε-containing GABAA receptors
    Jones, Brian L.
    Henderson, Leslie P.
    JOURNAL OF NEUROCHEMISTRY, 2007, 103 (03) : 1258 - 1271
  • [3] A novel site on γ3 subunits important for assembly of GABAA receptors
    Sarto, I
    Klausberger, T
    Ehya, N
    Mayer, B
    Fuchs, K
    Sieghart, W
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (34) : 30656 - 30664
  • [4] Assembly of functional α6β3γ2δ GABAA receptors in vitro
    Hevers, W
    Korpi, ER
    Lüddens, H
    NEUROREPORT, 2000, 11 (18) : 4103 - 4106
  • [5] Review: The influence of ethanol on the functional status of GABAA receptors
    Golovko, A.I.
    Golovko, S.I.
    Leont'eva, L.V.
    Zefirov, S.Yu.
    Biokhimiya, 2002, 67 (07): : 869 - 881
  • [6] The GABAA receptors
    Mohler, H
    Benke, D
    Fritschy, JM
    MOLECULAR AND CELLULAR TARGETS FOR ANTI-EPILEPTIC DRUGS, 1997, 12 : 39 - 53
  • [7] The emergence of antidepressant drugs targeting GABAA receptors: A concise review
    Gonda, Xenia
    Tarazi, Frank I.
    Dome, Peter
    BIOCHEMICAL PHARMACOLOGY, 2024, 228
  • [8] Trafficking of 5-HT3 and GABAA receptors (Review)
    Connolly, C. N.
    MOLECULAR MEMBRANE BIOLOGY, 2008, 25 (04) : 293 - 301
  • [9] Axonal GABAA receptors
    Trigo, Federico F.
    Marty, Alain
    Stell, Brandon M.
    EUROPEAN JOURNAL OF NEUROSCIENCE, 2008, 28 (05) : 841 - 848
  • [10] An update on GABAA receptors
    Mehta, AK
    Ticku, MK
    BRAIN RESEARCH REVIEWS, 1999, 29 (2-3) : 196 - 217