ARTICLE

COS Cells Expression Cloning of Tyrosine-phosphorylated Proteins by Immunocytochemistry

Correspondence to: Cesario Bianchi, Dept. of Surgery/Div. of Cardiothoracic Surgery, Beth Israel Deaconess Medical Center, 330 Brookline Ave. #DA-853, Boston, MA 02215. E-mail: cbianchi@caregroup.harvard.edu

Tyrosine phosphorylation is an important post-translational modification of proteins, essential in many aspects of the cell economy, particularly in signal transduction pathways. Despite the importance of protein tyrosine phosphorylation, the approaches available for molecular cloning remain limited. We have developed a COS cell-based eukaryotic expression cloning procedure for phosphotyrosine-containing proteins by immunocytochemistry of cell monolayers. The approach takes advantage of the low basal levels of tyrosine phosphorylated, robust transient expression, availability of specific antibodies against tyrosine-phosphorylated residues, and rescue of episomal DNA after immunocytochemistry. The technique is validated by cloning the rat proto-oncogene c-fgr in its tyrosine-phosphorylated form out of a rat kidney cDNA library containing over 10⁶ primary recombinants. This technique set the grounds for expression cloning of tyrosine-phosphorylated proteins in eukaryotic cells, and it is anticipated that further modifications and refinements will allow the identification of protein tyrosine phosphatase substrates. (J Histochem Cytochem 48:1097–1101, 2000)

Key Words: molecular cloning, COS, tyrosine phosphorylation, kinases, phosphatases, expression cloning, immunocytochemistry

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