Literature DB >> 3769922

Selective preparation and characterization of membranous and soluble forms of alkaline phosphatase from rat tissues. A comparison with the serum enzyme.

A Miki, Y Tanaka, S Ogata, Y Ikehara.   

Abstract

We developed a method for selective preparation of two forms of alkaline phosphatase from rat tissues. The enzyme was extracted by n-butanol treatment at pH 5.5 and pH 8.5 as soluble and aggregated (membranous) forms, respectively. The soluble form prepared from liver was found to be identical with the serum enzyme. Complete solubilization of the membrane-bound enzyme without detergents had a great advantage in its purification. Rat hepatoma AH-130 cells enriched in alkaline phosphatase were first used for purification of the liver-type enzyme. The hepatoma enzyme, purified by chromatographies on concanavalin-A-Sepharose, Sephacryl S-300 and hydroxyapatite was used for production of antibodies specific for the liver-type isozyme. An immunoaffinity column, prepared with anti-(hepatoma-enzyme) IgG was utilized for the enzyme purification from other tissues including the membranous form. Analyses of amino acid composition of the purified enzymes revealed that all the liver-type enzymes from hepatoma, liver, kidney and serum had the same composition, whereas the intestinal type consisted of the composition distinctly different from that in the liver type. In addition, there was no significant difference in amino acid composition between the soluble and membranous forms, suggesting a possible involvement in the membranous form of a hydrophobic component other than its polypeptide domain. The present method for selective preparation of the soluble and membranous forms of alkaline phosphatase will be useful for a further investigation on the interaction of the enzyme with membranes.

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Year:  1986        PMID: 3769922     DOI: 10.1111/j.1432-1033.1986.tb09937.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  8 in total

1.  Possible interference between tissue-non-specific alkaline phosphatase with an Arg54-->Cys substitution and acounterpart with an Asp277-->Ala substitution found in a compound heterozygote associated with severe hypophosphatasia.

Authors:  M Fukushi-Irié; M Ito; Y Amaya; N Amizuka; H Ozawa; S Omura; Y Ikehara; K Oda
Journal:  Biochem J       Date:  2000-06-15       Impact factor: 3.857

2.  Identification of glycosylphosphatidylinositol-specific phospholipases C in mouse brain membranes.

Authors:  F Fouchier; T Baltz; G Rougon
Journal:  Biochem J       Date:  1990-07-15       Impact factor: 3.857

3.  Possible mechanism of inhibition of cartilage alkaline phosphatase by insulin.

Authors:  C Gazzarrini; N Stagni; P Pollesello; P D'Andrea; B De Bernard
Journal:  Acta Diabetol Lat       Date:  1989 Oct-Dec

4.  Induction of glomerular alkaline phosphatase after challenge with lipopolysaccharide.

Authors:  Jola J Kapojos; Klaas Poelstra; Theo Borghuis; Anke Van Den Berg; Hans J Baelde; Pieter A Klok; Winston W Bakker
Journal:  Int J Exp Pathol       Date:  2003-06       Impact factor: 1.925

5.  Structure of the glycosylphosphatidylinositol membrane anchor of human placental alkaline phosphatase.

Authors:  C A Redman; J E Thomas-Oates; S Ogata; Y Ikehara; M A Ferguson
Journal:  Biochem J       Date:  1994-09-15       Impact factor: 3.857

6.  Vitamin D3 differentially regulates parathyroid hormone/parathyroid hormone-related peptide receptor expression in bone and cartilage.

Authors:  N Amizuka; M Y Kwan; D Goltzman; H Ozawa; J H White
Journal:  J Clin Invest       Date:  1999-02       Impact factor: 14.808

7.  Conversion of secretory proteins into membrane proteins by fusing with a glycosylphosphatidylinositol anchor signal of alkaline phosphatase.

Authors:  K Oda; J Cheng; T Saku; N Takami; M Sohda; Y Misumi; Y Ikehara; J L Millán
Journal:  Biochem J       Date:  1994-07-15       Impact factor: 3.857

8.  Primary structure of rat liver alkaline phosphatase deduced from its cDNA.

Authors:  Y Misumi; K Tashiro; M Hattori; Y Sakaki; Y Ikehara
Journal:  Biochem J       Date:  1988-02-01       Impact factor: 3.857

  8 in total

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