Partial purification and characterization of phosphotyrosyl-protein phosphatase from Ehrlich ascites tumor cells

• Published in: Biochemistry (Easton) Vol. 21; no. 22; pp. 5577 - 5584
• Main Authors: Hoerlein, Dietrich, Gallis, Byron, Brautigan, David L, Bornstein, Paul
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 01.10.1982
• Subjects: Alkaline Phosphatase - metabolism; Animals; Carcinoma, Ehrlich Tumor - enzymology; Edetic Acid - pharmacology; Ehrlich ascites tumor cells; Hydrogen-Ion Concentration; Mice; Phosphoprotein Phosphatases - metabolism; Phosphorylation; phosphotyrosyl-protein phosphatase; purification; Sodium Fluoride - pharmacology; Substrate Specificity; Tyrosine - metabolism; Zinc - pharmacology
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi00265a030

We have previously described a phosphotyrosylprotein phosphatase in membrane vesicles from human epidermoid carcinoma A431 cells which is inhibited by micromolar concentration of Zn2+ and is insensitive to ethylenediaminetetraacetic acid (EDTA) and NaF [Brautigan, D. L., Bornstein, P., & Gallis, B. (1981) J. Biol. Chem. 256, 6519-6522]. Here we present the identification and partial purification of a similar enzyme from lysates of Ehrlich ascites tumor cells. the enzyme was purified by using diethylaminoethyl-Sephadex, Zn2+ affinity, and Sephadex G-75 chromatography. During purification, the phosphatase was separated into at least three fractions, all of which exhibited very similar properties and an apparent molecular weight of 40 000 upon gel filtration. The enzyme dephosphorylated phosphotyrosine (P-Tyr)-containing carboxymethylated and succinylated (CM-SC) phosphorylase with an apparent Km of 0.8 microM, as well as P-Tyr containing casein and epidermal growth factor (EGF) receptor kinase, but did not dephosphorylate P-Ser-phosphorylase. The phosphatase was inhibited by Zn2+ at micromolar concentrations (K0.5 with EGF receptor kinase = 5 X 10(-6) M; with CM-SC phosphorylase = 3.3 X 10(-5) M) but not by millimolar concentrations of EDTA and NaF. No inhibition was seen with 1 mM tetramisole, a specific inhibitor of alkaline phosphatases. P-Tyr inhibited the enzyme by 50% at 0.4 X 10(-3) M, while Tyr, Pi, PPi, and p-nitrophenyl phosphate, an excellent substrate for alkaline phosphatases and structurally very similar to P-Tyr, exerted partial inhibition at concentrations above 10(-3) M. The pH optimum was found to be 6.5-7, depending on the substrate used. Very little activity was seen below pH 5 and above pH 8.5. These properties clearly distinguish this enzyme from alkaline phosphatases, as well as the neutral and acidic protein phosphatases so far described, and therefore define it as a new enzyme of the phosphatase family--a phosphotyrosyl-protein phosphatase.