Journal article
Purification, immunochemical characterization, and immunohistochemical localization of rat hepatic aryl sulfotransferase IV
Molecular pharmacology, Vol.40(1), pp.36-44
1991
DOI: 10.1016/S0026-895X(25)12849-6
PMID: 1857339
Abstract
Aryl sulfotransferases catalyze the formation of sulfuric acid esters from a diverse group of endogenous and xenobiotic organic chemicals. The isoenzyme of aryl sulfotransferase in livers of male Sprague-Dawley rats that exhibits the most varied substrate specificity is aryl sulfotransferase IV. A new method for the purification to homogeneity of aryl sulfotransferase IV was developed that, when compared with previously described procedures, provided a greater than 10-fold increase in total yield of enzyme/g of tissue. Homogeneous aryl sulfotransferase IV was used to prepare polyclonal antibodies in male New Zealand White rabbits. Results of immunochemical analyses demonstrated that these antibodies reacted with only a single protein in rat hepatic 100,000 x g supernatant fractions and, further, that the immunoreactive protein had the isoelectric point and subunit molecular mass characteristic of aryl sulfotransferase IV. Immunohistochemical analyses demonstrated that aryl sulfotransferase IV is present in hepatocytes throughout the liver, although centrilobular cells contain a significantly greater (p less than 0.01) amount of aryl sulfotransferase IV than do either midzonal or periportal cells, in which similar levels of the enzyme are found.
Details
- Title: Subtitle
- Purification, immunochemical characterization, and immunohistochemical localization of rat hepatic aryl sulfotransferase IV
- Creators
- Michael W Duffel - Univ. Iowa, coll. pharmacy, div. medicinal natural products chemistry, Iowa city IA 52242, United StatesThomas P Binder - Univ. Iowa, coll. pharmacy, div. medicinal natural products chemistry, Iowa city IA 52242, United StatesLynn Hosie - Univ. Iowa, coll. pharmacy, div. medicinal natural products chemistry, Iowa city IA 52242, United StatesHolly A Baden - Univ. Iowa, coll. pharmacy, div. medicinal natural products chemistry, Iowa city IA 52242, United StatesJill A Sanders - Univ. Iowa, coll. pharmacy, div. medicinal natural products chemistry, Iowa city IA 52242, United StatesShirley A Knapp - Univ. Iowa, coll. pharmacy, div. medicinal natural products chemistry, Iowa city IA 52242, United StatesJeffrey Baron - Univ. Iowa, coll. pharmacy, div. medicinal natural products chemistry, Iowa city IA 52242, United States
- Resource Type
- Journal article
- Publication Details
- Molecular pharmacology, Vol.40(1), pp.36-44
- Publisher
- American Society for Pharmacology and Experimental Therapeutics
- DOI
- 10.1016/S0026-895X(25)12849-6
- PMID
- 1857339
- ISSN
- 0026-895X
- eISSN
- 1521-0111
- Language
- English
- Date published
- 1991
- Academic Unit
- Pharmaceutical Sciences and Experimental Therapeutics; Neuroscience and Pharmacology; Medicinal and Natural Products Chemistry
- Record Identifier
- 9984303285502771
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