Kane Susan, Sano Hiroyuki, Liu Simon C H, Asara John M, Lane William S, Garner Charles C, Lienhard Gustav E
Department of Biochemistry, Dartmouth Medical School, Hanover, New Hampshire 03755, USA.
J Biol Chem. 2002 Jun 21;277(25):22115-8. doi: 10.1074/jbc.C200198200. Epub 2002 May 6.
This study describes a method for the identification of the substrates of specific serine kinases. An antibody specific for the phosphomotif generated by the kinase is used to isolate phosphorylated substrates by immunoprecipitation, and the isolated proteins are identified by tandem mass spectrometry of peptides. This method was applied to the identification of substrates for the protein kinase Akt, which specifically phosphorylates the RXRXXS/T motif. 3T3-L1 adipocytes were treated with insulin to activate Akt, and the putative Akt substrate proteins were isolated by immunoprecipitation with an antibody against the phospho form of this motif. This led to the identification of a novel 160-kDa substrate for Akt. The 160-kDa substrate for Akt, which was designated AS160, has a Rab GAP domain. Recombinant AS160 was shown to be a substrate for Akt, and two sites of phosphorylation, both in RXRXXS/T motifs, were identified by mass spectrometry and mutation. Insulin treatment of adipocytes caused AS160 to redistribute from the low density microsomes to the cytosol.
本研究描述了一种鉴定特定丝氨酸激酶底物的方法。使用对该激酶产生的磷酸化基序具有特异性的抗体,通过免疫沉淀分离磷酸化底物,并通过肽段串联质谱鉴定分离出的蛋白质。该方法应用于鉴定蛋白激酶Akt的底物,Akt特异性磷酸化RXRXXS/T基序。用胰岛素处理3T3-L1脂肪细胞以激活Akt,并用针对该基序磷酸化形式的抗体通过免疫沉淀分离推定的Akt底物蛋白。这导致鉴定出一种新的Akt 160 kDa底物。Akt的160 kDa底物被命名为AS160,具有Rab GAP结构域。重组AS160被证明是Akt的底物,通过质谱和突变鉴定出两个磷酸化位点,均位于RXRXXS/T基序中。用胰岛素处理脂肪细胞导致AS160从低密度微粒体重新分布到细胞质中。