PURIFICATION OF HUMAN LIVER FUMARYLACETOACETASE USING IMMUNOAFFINITY CHROMATOGRAPHY

被引:2
作者
VANFAASSEN, H [1 ]
VANDENBERG, IET [1 ]
BERGER, R [1 ]
机构
[1] UNIV GRONINGEN,DEPT PEDIAT,10 BLOEMSINGEL,9712 KZ GRONINGEN,NETHERLANDS
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 1990年 / 20卷 / 04期
关键词
Fumarylacetoacetase; Hydrolase; Immunoaffinity chromatography; Protein/enzyme purification; Tyrosine; Tyrosinemia type I;
D O I
10.1016/0165-022X(90)90093-R
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A method is described to purify fumarylacetoacetase from crude human liver extracts using immunoaffinity chromatography. Immobilized rabbit antibodies specific for beef liver fumarylacetoacetase were used as an immunoadsorbent. With this rapid and specific procedure human liver fumarylacetoacetase could be purified to apparent homogeneity. The molecular weight of native human liver fumarylacetoacetase is approximately 83000 as estimated by gel filtration. The two subunits have a molecular weight of approximately 41000, as determined by sodium dodecyl sulphate polyacrylamide gel electrophoresis. Purified human liver fumarylacetoacetase has a broad pH optimum with a maximum at pH 7.2 and a Km = 2.1 μM towards fumarylacetoacetate. © 1990.
引用
收藏
页码:317 / 324
页数:8
相关论文
共 15 条
[1]   DEFICIENCY OF FUMARYLACETOACETASE IN A PATIENT WITH HEREDITARY TYROSINEMIA [J].
BERGER, R ;
SMIT, GPA ;
STOKERDEVRIES, SA ;
DURAN, M ;
KETTING, D ;
WADMAN, SK .
CLINICA CHIMICA ACTA, 1981, 114 (01) :37-44
[2]   BIOCHEMICAL-STUDIES ON THE ENZYMATIC DEFICIENCIES IN HEREDITARY TYROSINEMIA [J].
BERGER, R ;
VANFAASSEN, H ;
SMITH, GPA .
CLINICA CHIMICA ACTA, 1983, 134 (1-2) :129-141
[3]   TYPE-I TYROSINEMIA - LACK OF IMMUNOLOGICALLY DETECTABLE FUMARYLACETOACETASE ENZYME PROTEIN IN TISSUES AND CELL-EXTRACTS [J].
BERGER, R ;
VANFAASSEN, H ;
TAANMAN, JW ;
DEVRIES, H ;
AGSTERIBBE, E .
PEDIATRIC RESEARCH, 1987, 22 (04) :394-398
[4]  
Berger R, 1985, INHERITED DIS AMINO, P192
[5]   4-HYDROXYPHENYLPYRUVIC ACID OXIDASE DEFICIENCY WITH NORMAL FUMARYLACETOACETASE - A NEW VARIANT FORM OF HEREDITARY HYPERTYROSINEMIA [J].
ENDO, F ;
KITANO, A ;
UEHARA, I ;
NAGATA, N ;
MATSUDA, I ;
SHINKA, T ;
KUHARA, T ;
MATSUMOTO, I .
PEDIATRIC RESEARCH, 1983, 17 (02) :92-96
[6]  
FURUKAWA N, 1984, PEDIATR RES, V18, P463, DOI 10.1203/00006450-198405000-00014
[7]   PURIFICATION AND PROPERTIES OF A DIKETO ACID HYDROLASE FROM BEEF LIVER [J].
HSIANG, HH ;
SCHMIDT, DE ;
SIM, SS ;
MAHURAN, DJ .
BIOCHEMISTRY, 1972, 11 (11) :2098-&
[8]   ASSAY OF FUMARYLACETOACETATE FUMARYLHYDROLASE IN HUMAN-LIVER - DEFICIENT ACTIVITY IN A CASE OF HEREDITARY TYROSINEMIA [J].
KVITTINGEN, EA ;
JELLUM, E ;
STOKKE, O .
CLINICA CHIMICA ACTA, 1981, 115 (03) :311-319
[9]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[10]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265