SAP102, a novel postsynaptic protein that interacts with NMDA receptor complexes in vivo

被引:371
作者
Muller, BM
Kistner, U
Kindler, S
Chung, WJ
Kuhlendahl, S
Fenster, SD
Lau, LF
Veh, RW
Huganir, RL
Gundelfinger, ED
Garner, CC
机构
[1] UNIV ALABAMA,NEUROBIOL RES CTR,BIRMINGHAM,AL 35213
[2] JOHNS HOPKINS UNIV,SCH MED,HOWARD HUGHES MED INST,DEPT NEUROSCI,BALTIMORE,MD 21205
[3] UNIV HAMBURG,INST CELLULAR BIOCHEM & CLIN NEUROBIOL,D-22529 HAMBURG,GERMANY
[4] INST NEUROBIOL,D-39008 MAGDEBURG,GERMANY
[5] YALE UNIV,SCH MED,HOWARD HUGHES MED INST,NEW HAVEN,CT 06510
[6] YALE UNIV,SCH MED,DEPT CELL BIOL,NEW HAVEN,CT 06510
[7] YALE UNIV,SCH MED,DEPT PHARMACOL,NEW HAVEN,CT 06510
关键词
D O I
10.1016/S0896-6273(00)80157-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Synapse-associated proteins (SAPs) are constituents of the pre- and postsynaptic submembraneous cytomatrix. Here, we present SAP102, a novel 102 kDa SAP detected in dendritic shafts and spines of asymmetric type 1 synapses. SAP102 is enriched in preparations of synaptic junctions, where it biochemically behaves as a component of the cortical cytoskeleton. Antibodies directed against NMDA receptors coimmunoprecipitate SAP102 from rat brain synaptosomes. Recombinant proteins containing the carboxy-terminal tail of NMDA receptor subunit NR2B interact with SAP102 from rat brain homogenates. All three PDZ domains in SAP102 bind the cytoplasmic tail of NR2B in vitro. These data represent direct evidence that in vivo SAP102 is involved in linking NMDA receptors to the submembraneous cytomatrix associated with postsynaptic densities at excitatory synapses.
引用
收藏
页码:255 / 265
页数:11
相关论文
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