Identification of Phosphorylated 422(aP2) Protein as pp15, the 15-kilodalton Target of the Insulin Receptor Tyrosine Kinase in 3T3-L1 Adipocytes

[32P]pp15, the [32P]phosphorylated form of a specific cytosolic substrate of the insulin receptor tyrosine kinase, was purified to homogeneity from mouse 3T3-L1 adipocytes incubated with 32Pi. Evidence presented here and previously indicates that pp15 contains a single phosphotyrosine residue. Alkyl...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1988-12, Vol.85 (23), p.8835-8839
Hauptverfasser: Hresko, Richard C., Bernier, Michel, Hoffman, Robert D., Flores-Riveros, Jaime R., Liao, Kan, Laird, Don M., Lane, M. Daniel
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Sprache:eng
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Zusammenfassung:[32P]pp15, the [32P]phosphorylated form of a specific cytosolic substrate of the insulin receptor tyrosine kinase, was purified to homogeneity from mouse 3T3-L1 adipocytes incubated with 32Pi. Evidence presented here and previously indicates that pp15 contains a single phosphotyrosine residue. Alkylated [32P]pp15 was subjected to limited digestion with trypsin, after which three incompletely digested tryptic [32P]phosphopeptides were purified for analysis. Amino acid and radiochemical sequence analysis of the [32P]phosphopeptides revealed that pp15 is the phosphorylation product of 422(aP2) protein, a 15-kDa adipocyte protein previously sequenced in this laboratory from the corresponding cDNA.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.85.23.8835