| Literature DB >> 15255944 |
Michaela Soltau1, Kerstin Berhörster, Stefan Kindler, Fritz Buck, Dietmar Richter, Hans-Jürgen Kreienkamp.
Abstract
The insulin receptor substrate of 53 kDa (IRSp53) is a target of the small GTPase cdc42 which is strongly enriched in the postsynaptic density of excitatory synapses. IRSp53 interacts with the postsynaptic shank1 scaffolding molecule in a cdc42 regulated manner. The functional significance of the cdc42/IRSp53 pathway in postsynaptic sites is however, unclear. Here we identify PSD-95 as a second synaptic interaction partner of IRSp53. Interaction is mediated by a C-terminal PDZ binding motif in IRSp53 and the second PDZ domain of PSD-95. In HEK cells, overexpressed IRSp53 induces filopodia and targets PSD-95 into these processes. Immunoprecipitation and immunocytochemistry experiments demonstrate that the interaction occurs at postsynaptic sites in the brain. By virtue of its PDZ-binding and SH3 domains, IRSp53 is capable of inducing the formation of a triple complex (shank1/IRSp53/PSD-95).Entities:
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Year: 2004 PMID: 15255944 DOI: 10.1111/j.1471-4159.2004.02523.x
Source DB: PubMed Journal: J Neurochem ISSN: 0022-3042 Impact factor: 5.372