Identification of a proline-rich Akt substrate as a 14-3-3 binding partner

被引:278
作者
Kovacina, KS
Park, GY
Bae, SS
Guzzetta, AW
Schaefer, E
Birnbaum, MJ
Roth, RA [1 ]
机构
[1] Stanford Univ, Dept Mol Pharmacol, Stanford, CA 94305 USA
[2] Univ Penn, Sch Med, Howard Hughes Med Inst, Philadelphia, PA 19104 USA
[3] Thermo Finnigan, San Jose, CA 95134 USA
[4] Hopkinton Div BioSource Int, Hopkinton, MA 01748 USA
关键词
D O I
10.1074/jbc.M210837200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Akt (also called protein kinase B) is one of the major downstream targets of the phosphatidylinositol 3-kinase pathway. This protein kinase has been implicated in insulin signaling, stimulation of cellular growth, and inhibition of apoptosis as well as transformation of cells. Although a number of cellular proteins have been identified as putative targets of the enzyme, additional substrates may play a role in the varied responses elicited by this enzyme. We have used a combination of 14-3-3 binding and recognition by an antibody to the phosphorylation consensus of the enzyme to identify and isolate one of the major substrates of Akt, which is also a 14-3-3 binding protein. This 40-kDa protein, designated PRAS40, is a proline-rich Akt substrate. Demonstration that it is a substrate of Akt was accomplished by showing that 1) PRAS40 was phosphorylated in vitro by purified Akt on the same site that was phosphorylated in insulin-treated cells; 2) activation of an inducible Akt was alone sufficient to stimulate the phosphorylation of PRAS40; and 3) cells lacking Akt1 and Akt2 exhibit a diminished ability to phosphorylate this protein. Thus, PRAS40 is a novel substrate of Akt, the phosphorylation of which leads to the binding of this protein to 14-3-3.
引用
收藏
页码:10189 / 10194
页数:6
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