The association of insulin-elicited phosphotyrosine proteins with src homology 2 domains

• Published in: The Journal of biological chemistry 1992-06, Vol.267 (16), p.11631-11636
• Main Authors: LAVAN, B. E, KUHNE, M. R, GARNER, C. W, ANDERSON, D, REEDIJK, M, PAWSON, T, LIENHARD, G. E
• Format: Article
• Language: English
• Subjects: 3T3 Cells; Amino Acid Sequence; Animals; Biological and medical sciences; Blotting, Western; Electrophoresis, Polyacrylamide Gel; Fundamental and applied biological sciences. Psychology; GTPase-Activating Proteins; Insulin - metabolism; Interactions. Associations; Intermolecular phenomena; Mice; Molecular biophysics; Molecular Sequence Data; Oncogene Protein pp60(v-src) - genetics; Phosphatidylinositol 3-Kinases; Phosphotransferases - metabolism; Phosphotyrosine; Precipitin Tests; Proteins - metabolism; ras GTPase-Activating Proteins; Receptor, Insulin - metabolism; Sequence Homology, Nucleic Acid; Substrate Specificity; Type C Phospholipases - metabolism; Tyrosine - analogs & derivatives; Tyrosine - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(19)49958-4

The interactions of the phosphotyrosine (Tyr(P))-containing proteins in basal and insulin-stimulated 3T3-L1 adipocytes with src homology 2 (SH2) domains from phosphatidylinositol 3-kinase (PI3K), ras GTPase-activating protein (GAP), and phospholipase C gamma have been examined. The Tyr(P) forms of the insulin receptor and its 160-kDa substrate protein (pp160) associated with fusion proteins containing either or both the SH2 domains of PI3K, but not with fusion proteins containing the two SH2 domains of GAP or phospholipase C gamma. These results demonstrate a specificity for the association of the Tyr(P) form of the insulin receptor and pp160 with SH2 domains that parallels the reported effects of insulin on PI3K, GAP, and phospholipase C gamma in vivo. Immunoprecipitates of pp160 from the cytosol of insulin-treated, but not basal, 3T3-L1 adipocytes contained PI3K activity. Moreover, the Tyr(P) form of pp160 with associated PI3K activity migrated at 10 S on a sucrose velocity gradient, whereas the Tyr(P) form without associated activity migrated at 6 S. These findings indicate that the Tyr(P) form of pp160 associates directly with PI3K in vivo.