Toponomics Analysis of Functional Interactions of the Ubiquitin Ligase PAM (Protein Associated with Myc) during Spinal Nociceptive Processing
| Autor: | Wiebke Becker, Sandra Pierre, Klaus Scholich, Claus Wittpoth, Gerd Geisslinger, Sabrina M. Holland, Achim Schmidtko, Christian Maeurer, Ovidiu Coste |
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| Rok vydání: | 2008 |
| Předmět: |
RNA Splicing
Receptor Metabotropic Glutamate 5 Ubiquitin-Protein Ligases Pain Syntaxin 1 Receptors Metabotropic Glutamate Proteomics Receptors N-Methyl-D-Aspartate Biochemistry Antibodies Analytical Chemistry Protein–protein interaction Rats Sprague-Dawley stomatognathic system Ubiquitin Tuberous Sclerosis Complex 2 Protein parasitic diseases Animals Receptors AMPA Molecular Biology Actin biology Tumor Suppressor Proteins Reproducibility of Results Colocalization Subcellular localization Actin cytoskeleton Actins Protein Structure Tertiary Rats Ubiquitin ligase Cell biology Protein Transport Spinal Cord biology.protein Adenylyl Cyclases Protein Binding |
| Zdroj: | Molecular & Cellular Proteomics. 7:2475-2485 |
| ISSN: | 1535-9476 |
| DOI: | 10.1074/mcp.m800201-mcp200 |
| Popis: | Protein associated with Myc (PAM) is a giant E3 ubiquitin ligase of 510 kDa. Although the role of PAM during neuronal development is well established, very little is known about its function in the regulation of synaptic strength. Here we used multiepitope ligand cartography (MELC) to study protein network profiles associated with PAM during the modulation of synaptic strength. MELC is a novel imaging technology that utilizes biomathematical tools to describe protein networks after consecutive immunohistochemical visualization of up to 100 proteins on the same sample. As an in vivo model to modulate synaptic strength we used the formalin test, a common model for acute and inflammatory pain. MELC analysis was performed with 37 different antibodies or fluorescence tags on spinal cord slices and led to the identification of 1390 PAM-related motifs that distinguish untreated and formalin-treated spinal cords. The majority of these motifs related to ubiquitin-dependent processes and/or the actin cytoskeleton. We detected an intermittent colocalization of PAM and ubiquitin with TSC2, a known substrate of PAM, and the glutamate receptors mGluR5 and GLUR1. Importantly these complexes were detected exclusively in the presence of F-actin. A direct PAM/F-actin interaction was confirmed by colocalization and cosedimentation. The binding of PAM toward F-actin varied strongly between the PAM splice forms found in rat spinal cords. PAM did not ubiquitylate actin or alter actin polymerization and depolymerization. However, F-actin decreased the ubiquitin ligase activity of purified PAM. Because PAM activation is known to involve its translocation, the binding of PAM to F-actin may serve to control its subcellular localization as well as its activity. Taken together we show that defining protein network profiles by topological proteomics analysis is a useful tool to identify previously unknown protein/protein interactions that underlie synaptic processes. |
| Databáze: | OpenAIRE |
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