Chen L, Wang H, Vicini S, Olsen R W
Department of Molecular and Medical Pharmacology, University of California, Los Angeles, CA 90095, USA.
Proc Natl Acad Sci U S A. 2000 Oct 10;97(21):11557-62. doi: 10.1073/pnas.190133497.
A microtubule-associated protein, gamma-aminobutyric acid type A (GABA(A)) receptor-associated protein (GABARAP), was previously identified as binding to the intracellular domain of GABA(A) receptors by using the yeast two-hybrid screen. In the present work, immunofluorescent staining and green fluorescent protein-tagged receptor subunits showed that GABARAP is associated with and promotes the clustering of GABA(A) receptors in QT-6 quail fibroblasts. The tubulin-binding motif of GABARAP and the gamma2 subunit of the receptor are required. Disruption of microtubules prevents the clustering in a time-dependent manner. When green fluorescent protein-tagged alpha1 or gamma2 subunit coexpressed with beta2, gamma2L, and GABARAP was used, recordings from visually identified cells revealed that clustered GABA(A) receptor had an EC(50) of about 20 microM, vs. 5.7 microM for the diffuse receptor. Clustered receptors deactivated faster and desensitized slower than the diffuse receptors, because of decrease in the apparent affinity of GABA binding. Different properties for clustered receptors relative to unclustered receptors in heterologous cells suggest that homologous differences between extrasynaptic and synaptic clustered receptors in neurons may be due to the organization of the postsynaptic machinery.
一种微管相关蛋白,γ-氨基丁酸A型(GABA(A))受体相关蛋白(GABARAP),先前通过酵母双杂交筛选被鉴定为与GABA(A)受体的细胞内结构域结合。在本研究中,免疫荧光染色和绿色荧光蛋白标记的受体亚基表明,GABARAP与GABA(A)受体相关并促进其在QT-6鹌鹑成纤维细胞中的聚集。GABARAP的微管蛋白结合基序和受体的γ2亚基是必需的。微管的破坏以时间依赖的方式阻止聚集。当使用与β2、γ2L和GABARAP共表达的绿色荧光蛋白标记的α1或γ2亚基时,对视觉识别细胞的记录显示,聚集的GABA(A)受体的半数有效浓度(EC(50))约为20微摩尔,而弥散型受体为5.7微摩尔。由于GABA结合的表观亲和力降低,聚集的受体比弥散型受体失活更快且脱敏更慢。异源细胞中聚集受体相对于未聚集受体的不同特性表明,神经元中突触外和突触聚集受体之间的同源差异可能是由于突触后机制的组织所致。