Incorporation of a gephyrin-binding motif targets NMDA receptors to gephyrin-rich domains in HEK 293 cells

被引:15
作者
Kins, S [1 ]
Kuhse, J [1 ]
Laube, B [1 ]
Betz, H [1 ]
Kirsch, J [1 ]
机构
[1] Max Planck Inst Brain Res, Dept Neurochem, D-60528 Frankfurt, Germany
关键词
glycine receptor beta subunit; postsynaptic localization; sorting of membrane proteins; synapse formation; transmembrane topology;
D O I
10.1046/j.1460-9568.1999.00527.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The peripheral membrane protein gephyrin is essential for the postsynaptic localization of inhibitory glycine receptors (GlyRs), Binding of gephyrin to the GlyR beta subunit is mediated by a sequence motif located in the intracellular loop region connecting transmembrane segments 3 and 4. Here, insertion of this binding motif is shown to alter the subcellular distribution of an excitatory neurotransmitter receptor in transfected mammalian cells. Upon coexpression with gephyrin, a mutant N-methyl-D-aspartate (NMDA) receptor containing NMDA receptor 1 (NR1) subunits which harboured a gephyrin-binding motif within its cytoplasmic tail region, was targeted to intracellular gephyrin-rich domains, as previously observed for the GlyR beta subunit. Our data indicate that a gephyrin-binding motif located in a cytoplasmic domain of an integral membrane protein suffices for routing to gephyrin-rich domains.
引用
收藏
页码:740 / 744
页数:5
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