EAST, an Epidermal Growth Factor Receptor- and Eps15-associated Protein with Src Homology 3 and Tyrosine-based Activation Motif Domains

• Published in: The Journal of biological chemistry Vol. 273; no. 33; pp. 21408 - 21415
• Main Authors: Lohi, Olli, Poussu, Anssi, Meriläinen, Jari, Kellokumpu, Sakari, Wasenius, Veli-Matti, Lehto, Veli-Pekka
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 14-08-1998; American Society for Biochemistry and Molecular Biology
• Subjects: Amino Acid Sequence; Animals; Calcium-Binding Proteins - metabolism; Cells, Cultured; Chick Embryo; Cloning, Molecular; DNA, Complementary; ErbB Receptors - metabolism; Molecular Sequence Data; Phosphoproteins - chemistry; Phosphoproteins - genetics; Phosphoproteins - metabolism; Phosphorylation; RNA, Messenger - genetics; RNA, Messenger - metabolism; Sequence Homology, Amino Acid; Signal Transduction; src Homology Domains; Tyrosine - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.273.33.21408

We describe the cloning and characterization of a new cytoplasmic protein designated epidermal growth factor receptor-associated protein with SH3- andTAM domains (EAST). It contains an Src homology 3 domain in its midregion and a tyrosine-based activation motif in its COOH terminus. Antibodies to EAST recognize a 68-kDa protein that is present in most chicken tissues. An epidermal growth factor (EGF)-dependent association between the EGF receptor (EGFR) and EAST was shown by reciprocal immunoprecipitation/immunoblotting studies with specific antibodies. Activated EGFR catalyzed the tyrosine phosphorylation of EAST, as judged by an in vitro kinase assay with both immunoprecipitated and purified EGFR. Immunoprecipitation/immunoblotting experiments also demonstrated an association between EAST and eps15, an EGFR substrate associated with clathrin-coated pits and vesicles, which is essential in the endocytotic pathway. The association between EAST and eps15 was not affected by EGF treatment. In immunofluorescence microscopy, EAST was shown to partially colocalize with clathrin. The sequence of the NH2-terminal portion of EAST shows a high degree of similarity with a group of proteins involved in endocytosis or vesicle trafficking. Thus, EAST is a novel signal transduction component probably involved in EGF signaling and in the endocytotic machinery.