Home LiteratureArticle Details
PMID: 6139755 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Thermolabile and thermostable human platelet phenol sulfotransferase. Substrate specificity and physical separation.

Naunyn-Schmiedeberg's archives of pharmacology ·Vol. 324 ·No. 2 ·1983-09-00 ·Pages 140-7

Reiter C, Mwaluko G, Dunnette J, Van Loon J, Weinshilboum R

Abstract

Human platelets contain at least two forms of phenol sulfotransferase (PST), a thermolabile (TL) form for which dopamine is a substrate and a thermostable (TS) form for which micromolar concentrations of phenol can serve as substrate. At higher concentrations phenol is also a substrate for the TL form. Studies of the regulation and the possible clinical value of measurements of platelet PST have been hampered because there is no specific substrate for the TS form of the enzyme. The purposes of these experiments were to determine whether there might be a better substrate than phenol for use in measurement of the activity of the TS form of platelet PST, and to attempt to physically separate the two forms of the platelet enzyme. The results of substrate kinetic, thermal stability, and inhibitor studies performed with platelet homogenates were all compatible with the conclusion that p-nitrophenol and 6-OH-melatonin were substrates for both the TS and TL forms of platelet PST. Norepinephrine, epinephrine and 5-OH-tryptamine were substrates for only the TL form. The apparent Km constants of the two forms of PST for p-nitrophenol differed by 7,100-fold when measured in platelet homogenates. This difference was 200 times greater than that which has been reported for phenol. Therefore, p-nitrophenol is the preferred substrate for measurement of the TS PST activity if interference by the TL activity is to be avoided. This information made it possible to use p-nitrophenol as a substrate in experiments designed to separate the two forms of platelet PST.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
Arylsulfotransferase Blood Platelets/enzymology Chromatography, Ion Exchange Hot Temperature Humans Kinetics Melatonin/analogs & derivatives,metabolism Neurotransmitter Agents/metabolism Nitrophenols/metabolism Substrate Specificity Sulfurtransferases/analysis,antagonists & inhibitors,blood
Chemicals
Neurotransmitter Agents Nitrophenols Sulfurtransferases Arylsulfotransferase Melatonin 6-hydroxymelatonin 4-nitrophenol
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Reiter C
Mwaluko G
Dunnette J
Van Loon J
Weinshilboum R
References (20)
20 references, click to expand
  1. Statistical estimations in enzyme kinetics.
    Biochem J. 1961 Aug;80:324-32 PMID: 13785321
  2. Acetaminophen and phenol: substrates for both a thermostable and a thermolabile form of human platelet phenol sulfotransferase.
    J Pharmacol Exp Ther. 1982 Apr;221(1):43-51 PMID: 6950087
  3. alpha-Methyldopa, alpha-methyldopamine an alpha-methylnoradrenaline: substrates for the thermolabile form of human platelet phenol sulphotransferase.
    Br J Clin Pharmacol. 1982 Aug;14(2):231-9 PMID: 7049213
  4. Localization and characterization of phenol sulfotransferase in human platelets.
    Life Sci. 1979 Jan 8;24(2):125-30 PMID: 763073
  5. Phenolsulphotransferase: enzyme activity and endogenous inhibitors in the human erythrocyte.
    J Lab Clin Med. 1979 Jul;94(1):158-71 PMID: 469373
  6. Metabolism of exogenous melatonin in schizophrenic and non-schizophrenic volunteers.
    Clin Chim Acta. 1969 Nov;26(2):281-5 PMID: 4242832
  7. Pharmacokinetics of acetaminophen in the human neonate: formation of acetaminophen glucuronide and sulfate in relation to plasma bilirubin concentration and D-glucaric acid excretion.
    Pediatrics. 1975 Jun;55(6):818-25 PMID: 1134883
  8. Computer programmes for processing enzyme kinetic data.
    Nature. 1963 May 4;198:463-5 PMID: 14021666
  9. Multiple forms of phenolsulphotransferase in human tissues: selective inhibition by dichloronitrophenol.
    Biochem Pharmacol. 1982 May 15;31(10):1893-7 PMID: 6954952
  10. Plasma concentration of alpha-methyldopa and sulphate conjugate after oral administration of methyldopa and intravenous administration of methyldopa and methyldopa hydrochloride ethyl ester.
    Eur J Clin Pharmacol. 1975 Aug 14;8(6):381-6 PMID: 1233238
  11. Rat brain phenolsulfotransferase: partial purification and some properties.
    Biochim Biophys Acta. 1973 Dec 19;327(2):365-74 PMID: 4778939
  12. 3-Methoxy-4-hydroxyphenylglycol sulfate, a new metabolite of epinephrine and norepinephrine.
    Biochim Biophys Acta. 1959 Dec;36:576-7 PMID: 13795312
  13. Specific quantitation of urinary 6-hydroxymelatonin sulphate by gas chromatography mass spectrometry.
    Biomed Mass Spectrom. 1980 Feb;7(2):84-7 PMID: 7407336
  14. Selective monoamine oxidase inhibitor drugs as aids in evaluating the role of type A and B enzymes.
    Neuropharmacology. 1975 Nov;14(11):819-25 PMID: 1207877
  15. Platelet phenol sulfotransferase activity: correlation with sulfate conjugation of acetaminophen.
    Clin Pharmacol Ther. 1982 Nov;32(5):612-21 PMID: 6957279
  16. Human platelet phenol sulphotransferase: assay procedure, substrate and tissue correlations.
    Clin Chim Acta. 1981 Mar 5;110(2-3):157-67 PMID: 6939511
  17. Phenolsulphotransferase in human tissue: radiochemical enzymatic assay and biochemical properties.
    Clin Chim Acta. 1980 Apr 11;103(1):79-90 PMID: 6930336
  18. Platelet phenolsulphotransferase deficiency in dietary migraine.
    Lancet. 1982 May 1;1(8279):983-6 PMID: 6122845
  19. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.
    Anal Biochem. 1976 May 7;72:248-54 PMID: 942051
  20. Sulphate conjugation of biologically active monoamines and their metabolites by human platelet phenolsulphotransferase.
    Clin Chim Acta. 1981 Apr 9;111(2-3):247-56 PMID: 6939513
Article Info
Journal
Naunyn-Schmiedeberg's archives of pharmacology
Abbr.
Naunyn Schmiedebergs Arch Pharmacol
ISSN
0028-1298
Published
1983-09-00
Pages
140-7
Language
English
Region
Germany
NLM ID
0326264
Subset
IM
Grants
NIGMS NIH HHS · GM 28157 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com