Identification and analysis of glycogen synthase kinase 3 beta1 interactome

被引:22
作者
Gao, Xuejuan [1 ]
Wang, Jian-Ying [1 ]
Gao, Ling-Mei [1 ]
Yin, Xing-Feng [1 ]
Liu, Langxia [1 ]
机构
[1] Jinan Univ, Inst Life & Hlth Engn, Guangzhou 510632, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
<fixed-case>GSK</fixed-case>-31; <fixed-case>GST</fixed-case> pull-down; <fixed-case>LC</fixed-case>-<fixed-case>MS</fixed-case>; <fixed-case>MS</fixed-case>; protein-protein interaction; DIFFERENTIAL REGULATION; PROTEIN-KINASE; INTACT-CELLS; CANCER CELLS; HNRNP K; EXPRESSION; TRANSCRIPTION; 3-BETA; GLYCOGEN-SYNTHASE-KINASE-3; PHOSPHORYLATION;
D O I
10.1002/cbin.10095
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glycogen synthase kinase-3 beta (GSK3) was initially identified as a key protein in glucose metabolism. GSK3 might be involved in cell growth, motility and apoptosis. Systematic identification of GSK3-associated proteins is crucial for the exhaustive understanding of its functions. Using GST pull-down experiment and LCMS/MS analysis coupled to bioinformatics tools, we have identified 114 proteins that interacted with GSK31 in hepatocellular carcinoma HepG2 cells. Most of the identified proteins are implicated in metabolic process, whereas other proteins are important for cell proliferation or migration, and have been associated with cancer development and metastasis. Several representative proteins, such as hnRNPK, PCNA, Ezrin and STAT1, have been confirmed to interact with GSK-31 by co-immunoprecipitation in HepG2 cells. Further studies of these interactions may discover the precise roles and the underlying mechanisms of GSK-31 in tumour growth and metastasis.
引用
收藏
页码:768 / 779
页数:12
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