Characterization of the Localization and Function of Necap 1 in Neurons.
From: Department of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada.
Journal of neurochemistry
- Publish Date: Sep 2006
- ISSN: 0022-3042
- Volume: 98
- Issue: 6
- Pages: 1746-62
- Medium: Print
- Language: English
- Citation (JAMA): Murshid Ayesha, Srivastava Archana, Kumar Rohit, et al. Characterization of the Localization and Function of Necap 1 in Neurons.. J. Neurochem. Sep 2006;98:1746-62
Abstract
NECAPs (adaptin ear-binding clathrin-associated protein) are a new family of clathrin accessory proteins identified through a proteomic analysis of clathrin-coated vesicles (CCVs) from the brain. One member of this family, NECAP 1, is found primarily in tissues from the central nervous system and has been shown to be complexed tightly with a substantial portion of adaptor protein-2 (AP-2) in brain extracts. However, the function and intracellular location of this protein is unknown. In this study, we find that endogenous and epitope-tagged NECAP 1 co-localizes well with clathrin and AP-2 in punctate structures, many of which also contain the presynaptic markers synaptophysin, synaptotagmin or synaptic vesicle protein 2 (SV2). NECAP 1 was also detected by western blot in synaptic vesicle preparations. Overexpression of a truncation mutant of NECAP 1 (BC-NECAP 1) in neurons inhibited transferrin endocytosis but not epidermal growth factor (EGF) endocytosis, and this inhibition was dependent on an AP-2-binding WVQF motif. Moreover, overexpression of BC-NECAP 1 results in inhibition of synaptotagmin endocytosis both in unstimulated neurons and in neurons stimulated with potassium chloride. This inhibition was abrogated by truncation of the WVQF domain. We conclude from these observations that NECAP 1 plays a role in clathrin-mediated neuronal endocytosis, including a role in presynaptic endocytosis.
Mesh Headings (Keywords): Adaptor Protein Complex 2, Animals, Biological Markers, Cells, Cultured, Clathrin, Endocytosis, Epidermal Growth Factor, Epitopes, Gene Deletion, Hippocampus, Membrane Proteins, Neurons, Peptide Fragments, Potassium Chloride, Rats, Synapses, Synaptotagmins, Time Factors, Tissue Distribution, Transferrin
Check for Full Text / PubMed Unique Identifier (PMID): 16879712
This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.
Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.
The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.
