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Identification of VCP/p97, CHIP and amphiphysin II interaction partners using membrane-based human proteome arrays

Item Type:Article
Title:Identification of VCP/p97, CHIP and amphiphysin II interaction partners using membrane-based human proteome arrays
Creators Name:Grelle, G. and Kostka, S. and Otto, A. and Kersten, B. and Genser, K.F. and Mueller, E.C. and Waelter, S. and Boeddrich, A. and Stelzl, U. and Haenig, C. and Volkmer-Engert, R. and Landgraf, C. and Alberti, S. and Hoehfeld, J. and Stroedicke, M. and Wanker, E.E.
Abstract:Proteins mediate their biological function through interactions with other proteins. Therefore, the systematic identification and characterization of protein-protein interactions have become a powerful proteomic strategy to understand protein function and comprehensive cellular regulatory networks. For the screening of valosin-containing protein, carboxyl terminus of Hsp70-interacting protein (CHIP), and amphiphysin II interaction partners, we utilized a membrane-based array technology that allows the identification of human protein-protein interactions with crude bacterial cell extracts. Many novel interaction pairs such as valosin-containing protein/autocrine motility factor receptor, CHIP/caytaxin, or amphiphysin II/DLP4 were identified and subsequently confirmed by pull-down, two-hybrid and co-immunoprecipitation experiments. In addition, assays were performed to validate the interactions functionally. CHIP e.g. was found to efficiently polyubiquitinate caytaxin in vitro, suggesting that it might influence caytaxin degradation in vivo. Using peptide arrays, we also identified the binding motifs in the proteins DLP4, XRCC4, and fructose-1,6-bisphosphatase, which are crucial for the association with the Src homology 3 domain of amphiphysin II. Together these studies indicate that our human proteome array technology permits the identification of protein-protein interactions that are functionally involved in neurodegenerative disease processes, the degradation of protein substrates, and the transport of membrane vesicles.
Keywords:Adenosine Triphosphatases, Amino Acid Sequence, Artificial Membranes, Cell Cycle Proteins, Cercopithecus aethiops, COS Cells, HSC70 Heat-Shock Proteins, Molecular Sequence Data, Nerve Tissue Proteins, Protein Array Analysis, Protein Binding, Protein Interaction Mapping, Proteome, Tertiary Protein Structure, Animals
Source:Molecular & Cellular Proteomics
ISSN:1535-9476
Publisher:American Society for Biochemistry and Molecular Biology (U.S.A.)
Volume:5
Number:2
Page Range:234-244
Date:1 February 2006
Official Publication:https://doi.org/10.1074/mcp.M500198-MCP200
PubMed:View item in PubMed

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