A method to identify serine kinase substrates. Akt phosphorylates a novel adipocyte protein with a Rab GTPase-activating protein (GAP) domain. 2002

Susan Kane, and Hiroyuki Sano, and Simon C H Liu, and John M Asara, and William S Lane, and Charles C Garner, and Gustav E Lienhard
Department of Biochemistry, Dartmouth Medical School, Hanover, New Hampshire 03755, USA.

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.

UI MeSH Term Description Entries
D007328 Insulin A 51-amino acid pancreatic hormone that plays a major role in the regulation of glucose metabolism, directly by suppressing endogenous glucose production (GLYCOGENOLYSIS; GLUCONEOGENESIS) and indirectly by suppressing GLUCAGON secretion and LIPOLYSIS. Native insulin is a globular protein comprised of a zinc-coordinated hexamer. Each insulin monomer containing two chains, A (21 residues) and B (30 residues), linked by two disulfide bonds. Insulin is used as a drug to control insulin-dependent diabetes mellitus (DIABETES MELLITUS, TYPE 1). Iletin,Insulin A Chain,Insulin B Chain,Insulin, Regular,Novolin,Sodium Insulin,Soluble Insulin,Chain, Insulin B,Insulin, Sodium,Insulin, Soluble,Regular Insulin
D008861 Microsomes Artifactual vesicles formed from the endoplasmic reticulum when cells are disrupted. They are isolated by differential centrifugation and are composed of three structural features: rough vesicles, smooth vesicles, and ribosomes. Numerous enzyme activities are associated with the microsomal fraction. (Glick, Glossary of Biochemistry and Molecular Biology, 1990; from Rieger et al., Glossary of Genetics: Classical and Molecular, 5th ed) Microsome
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D010766 Phosphorylation The introduction of a phosphoryl group into a compound through the formation of an ester bond between the compound and a phosphorus moiety. Phosphorylations
D010957 Plasmids Extrachromosomal, usually CIRCULAR DNA molecules that are self-replicating and transferable from one organism to another. They are found in a variety of bacterial, archaeal, fungal, algal, and plant species. They are used in GENETIC ENGINEERING as CLONING VECTORS. Episomes,Episome,Plasmid
D011233 Precipitin Tests Serologic tests in which a positive reaction manifested by visible CHEMICAL PRECIPITATION occurs when a soluble ANTIGEN reacts with its precipitins, i.e., ANTIBODIES that can form a precipitate. Precipitin Test,Test, Precipitin,Tests, Precipitin
D011485 Protein Binding The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments. Plasma Protein Binding Capacity,Binding, Protein
D011518 Proto-Oncogene Proteins Products of proto-oncogenes. Normally they do not have oncogenic or transforming properties, but are involved in the regulation or differentiation of cell growth. They often have protein kinase activity. Cellular Proto-Oncogene Proteins,c-onc Proteins,Proto Oncogene Proteins, Cellular,Proto-Oncogene Products, Cellular,Cellular Proto Oncogene Proteins,Cellular Proto-Oncogene Products,Proto Oncogene Products, Cellular,Proto Oncogene Proteins,Proto-Oncogene Proteins, Cellular,c onc Proteins
D003600 Cytosol Intracellular fluid from the cytoplasm after removal of ORGANELLES and other insoluble cytoplasmic components. Cytosols
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

Susan Kane, and Hiroyuki Sano, and Simon C H Liu, and John M Asara, and William S Lane, and Charles C Garner, and Gustav E Lienhard
February 1998, The Journal of biological chemistry,
Susan Kane, and Hiroyuki Sano, and Simon C H Liu, and John M Asara, and William S Lane, and Charles C Garner, and Gustav E Lienhard
April 2017, Protein science : a publication of the Protein Society,
Susan Kane, and Hiroyuki Sano, and Simon C H Liu, and John M Asara, and William S Lane, and Charles C Garner, and Gustav E Lienhard
February 2007, Diabetes,
Susan Kane, and Hiroyuki Sano, and Simon C H Liu, and John M Asara, and William S Lane, and Charles C Garner, and Gustav E Lienhard
September 2006, Biochimica et biophysica acta,
Susan Kane, and Hiroyuki Sano, and Simon C H Liu, and John M Asara, and William S Lane, and Charles C Garner, and Gustav E Lienhard
January 2015, Methods in molecular biology (Clifton, N.J.),
Susan Kane, and Hiroyuki Sano, and Simon C H Liu, and John M Asara, and William S Lane, and Charles C Garner, and Gustav E Lienhard
September 2005, Biochemical and biophysical research communications,
Susan Kane, and Hiroyuki Sano, and Simon C H Liu, and John M Asara, and William S Lane, and Charles C Garner, and Gustav E Lienhard
May 2008, Diabetes,
Susan Kane, and Hiroyuki Sano, and Simon C H Liu, and John M Asara, and William S Lane, and Charles C Garner, and Gustav E Lienhard
October 2011, International journal of andrology,
Susan Kane, and Hiroyuki Sano, and Simon C H Liu, and John M Asara, and William S Lane, and Charles C Garner, and Gustav E Lienhard
July 1993, Biochemical and biophysical research communications,
Susan Kane, and Hiroyuki Sano, and Simon C H Liu, and John M Asara, and William S Lane, and Charles C Garner, and Gustav E Lienhard
June 2015, The Journal of cell biology,
Copied contents to your clipboard!