| Literature DB >> 15372503 |
Greg R Phillips1, Tonya R Anderson, Laurence Florens, Christopher Gudas, Gabriela Magda, John R Yates, David R Colman.
Abstract
CNS synapses are complex sites of cell-cell communication. Identification and characterization of the protein components of synapses will lead to a better understanding of the mechanisms of neurotransmission and plasticity. We applied multidimensional protein identification technology (MudPIT) to purified, guanidine-solubilized postsynaptic fractions to identify novel synaptically localized molecules. We identified several actin-associated proteins known to regulate actin polymerization and control cell motility in nonneural cells that have not previously been associated with CNS synaptic function. One of these is lasp-1, an actin-associated LIM and SH3 domain-containing protein. We show that lasp-1 is strongly expressed by CNS neurons and is concentrated at synaptic sites. Overall, the preponderance of actin-associated proteins in postsynaptic density fractions, and specifically those involved in actin reorganization, suggests that there are many modes by which the state of synaptic F-actin polymerization and, hence, synaptic physiology are affected. 2004 Wiley-Liss, Inc.Entities:
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Year: 2004 PMID: 15372503 DOI: 10.1002/jnr.20224
Source DB: PubMed Journal: J Neurosci Res ISSN: 0360-4012 Impact factor: 4.164