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Mapping the interactome of overexpressed RAF kinase inhibitor protein in a gastric cancer cell line.

AbstractBACKGROUND:
Gastric cancer (GC) is a threat to human health with increasing incidence and mortality worldwide. Down-regulation or absence of RAF kinase inhibitor protein (RKIP) was associated with the occurrence, differentiation, invasion, and metastasis of GC. This study aims to investigate the molecular mechanisms and biological functions of RKIP in the GC biology.
METHODS:
The fusion expression plasmid pcDNA3.1-RKIP-3xFLAG was transfected into SGC7901 cells, the RKIP fusion proteins were purified with anti-flag M2 magnetic beads, and the RKIP-interacting proteins were identified with tandem mass spectrometry (MS/MS), and were analyzed with bioinformatics tools. Western blot and co-immunoprecipitation were used to confirm the interaction complex.
RESULTS:
A total of 72 RKIP-interacting proteins were identified by MS/MS. Those proteins play roles in enzyme metabolism, molecular chaperoning, biological oxidation, cytoskeleton organization, signal transduction, and enzymolysis. Three RKIP-interaction protein network diagrams were constructed with Michigan Molecular Interactions, functional linage network, and Predictome analysis to address the molecular pathways of the functional activity of RKIP. The MS/MS-characterized components of the existing interaction complex (RKIP, HSP90, 14-3-3ε, and keratin 8) were confirmed by Western blot analysis and co-immunoprecipitation.
CONCLUSION:
This study is the first discovery of the interaction of RKIP with HSP90, 14-3-3, and keratin. The present data would provide insight into the molecular mechanisms of how RKIP inhibits the occurrence and development of GC.
AuthorsHuan Gu, Xianquan Zhan, Guiying Zhang, Lu Yan, William Cs Cho, Maoyu Li, Ting Liu, Zhuchu Chen
JournalBMC cancer (BMC Cancer) Vol. 13 Pg. 536 (Nov 09 2013) ISSN: 1471-2407 [Electronic] England
PMID24209905 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Carrier Proteins
  • PEBP1 protein, human
  • Phosphatidylethanolamine Binding Protein
Topics
  • Carrier Proteins (metabolism)
  • Cell Line, Tumor
  • Gene Expression
  • Humans
  • Phosphatidylethanolamine Binding Protein (genetics, metabolism)
  • Protein Binding
  • Protein Interaction Mapping (methods)
  • Protein Interaction Maps
  • Reproducibility of Results
  • Stomach Neoplasms (genetics, metabolism)
  • Transfection

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