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Identification of proteins interacting with the catalytic subunit of PP2A by proteomics
Author(s) -
Lee WonJeong,
Kim DongUk,
Lee MiYoung,
Choi KangYell
Publication year - 2007
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.200600480
Subject(s) - protein phosphatase 2 , protein subunit , immunoprecipitation , proteomics , proteome , phosphatase , biology , wnt signaling pathway , interactome , microbiology and biotechnology , phosphorylation , signal transduction , biochemistry , chemistry , gene
The protein phosphatase 2A (PP2A) is a serine/threonine phosphatase involved in the regulation of multiple signaling pathways including the Wnt/β‐catenin and the ERK pathways. To understand the complex signaling networking associated with PP2A, we searched proteins interacting with the catalytic subunit of protein phosphatase 2A (PP2Ac) by a pull‐down analysis followed by 2‐D gel electrophoresis and proteomic analyses. The probability of identification of the proteins interacting with PP2Ac was increased by searching proteins differently interacting with PP2Ac according to stimulation of Wnt3a, which regulates both the Wnt/β‐catenin and the ERK pathways. Around 100 proteins, pulled‐down by His‐tagged PP2Ac, were identified in 2‐D gels stained with CBB. By MALDI‐TOF‐MS analyses of 45 protein spots, we identified several proteins that were previously known to interact with PP2A, such as Axin and CaMK IV. In addition, we also identified many proteins that potentially interact with PP2Ac. The interactions of several candidate proteins, such as tuberous sclerosis complex 2, RhoB, R‐Ras, and Nm23H2, with PP2Ac, were confirmed by in vitro binding analyses and/or coimmunoprecipitation experiments.