Literature DB >> 2875937

Attenuated activities and structural alterations of arylsulfatase A in tissues from subjects with pseudo arylsulfatase A deficiency.

H Kihara, W E Meek, A L Fluharty.   

Abstract

It had been shown previously that arylsulfatase A activity was attenuated in pseudo arylsulfatase A deficiency fibroblasts and that subunits of the enzyme were smaller than subunits of the enzyme in normal fibroblasts. Attenuated enzyme activity has now been affirmed in other tissues. Subunits of the enzyme from these sources were also found to be smaller with apparent molecular size 59 and 56 kdaltons. Subunits of enzyme in corresponding control tissues were larger and there was heterogeneity in apparent molecular size as follows: fibroblasts, 63 and 59 kdaltons; liver, 63 and 59 kdaltons; kidney, 63 and 58 kdaltons; spleen, 63 and 58 kdaltons; placenta, 62 and 58 kdaltons; and urine, 61 and 57 kdaltons. Attenuated enzyme activity and structurally altered enzyme in pseudo arylsulfatase A deficiency appears to be systemic. However, the reason for reduced amounts of structurally altered enzyme with normal catalytic activity is unresolved.

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Year:  1986        PMID: 2875937     DOI: 10.1007/bf00278786

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  21 in total

1.  Inheritance of metachromatic leukodystrophy.

Authors:  U Langenbeck; P Dunker; R Heipertz; H Pilz
Journal:  Am J Hum Genet       Date:  1977-11       Impact factor: 11.025

2.  Microheterogeneity of arylsulfatase A from human tissues.

Authors:  R L Stevens; A L Fluharty; A R Killgrove; H Kihara
Journal:  Biochim Biophys Acta       Date:  1976-10-11

3.  Protein purification by affinity chromatography. Derivatizations of agarose and polyacrylamide beads.

Authors:  P Cuatrecasas
Journal:  J Biol Chem       Date:  1970-06       Impact factor: 5.157

4.  Metabolism of fatty acid-labeled cerebroside sulfate in cultured cells from controls and metachromatic leukodystrophy patients. Use in the prenatal identification of a false positive fetus.

Authors:  T Kudoh; M Sattler; J Malmstrom; M A Bitter; D A Wenger
Journal:  J Lab Clin Med       Date:  1981-11

5.  Purification and properties of arylsulfatase. A from human urine.

Authors:  R L Stevens; A L Fluharty; M H Skokut; H Kihara
Journal:  J Biol Chem       Date:  1975-04-10       Impact factor: 5.157

6.  Microheterogeneity of arylsulfatase a: Treatment with hydrolytic enzymes.

Authors:  T A Sarafian; A L Fluharty; H Kihara
Journal:  Biochem Med       Date:  1984-02

7.  Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophy.

Authors:  P L Chang; R G Davidson
Journal:  Proc Natl Acad Sci U S A       Date:  1983-12       Impact factor: 11.205

8.  Synthesis and maturation of cross-reactive glycoprotein in fibroblasts deficient in arylsulfatase A activity.

Authors:  G Bach; E F Neufeld
Journal:  Biochem Biophys Res Commun       Date:  1983-04-15       Impact factor: 3.575

9.  Prenatal diagnosis of pseudo arylsulphatase A deficiency.

Authors:  H Kihara; A L Fluharty; K K Tsay; R P Bachman; J D Stephens; W G Ng
Journal:  Prenat Diagn       Date:  1983-01       Impact factor: 3.050

10.  Two allelic forms of human arylsulfatase A with different numbers of asparagine-linked oligosaccharides.

Authors:  A Waheed; F Steckel; A Hasilik; K von Figura
Journal:  Am J Hum Genet       Date:  1983-03       Impact factor: 11.025

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  2 in total

1.  Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications.

Authors:  C Hohenschutz; P Eich; W Friedl; A Waheed; E Conzelmann; P Propping
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

2.  Extremely low arylsulfatase A enzyme activity does not necessarily cause symptoms: A long-term follow-up and review of the literature.

Authors:  Lucia Laugwitz; Vidiyaah Santhanakumaran; Mareike Spieker; Judith Boehringer; Benjamin Bender; Volkmar Gieselmann; Stefanie Beck-Woedl; Gernot Bruchelt; Klaus Harzer; Ingeborg Kraegeloh-Mann; Samuel Groeschel
Journal:  JIMD Rep       Date:  2022-05-04
  2 in total

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