A DE filter disk technique for assaying the activity of nucleotidase is described. This method is based on the observation that nucleotides bind to the filters at 5 mM Tris-HCl (pH 7.8) while nucleosides do not. As parameter for the nucleotidase activity the decrease of bound nucleotides is determin
Paper disk assay for glycosaminoglycan sulfotransferases
β Scribed by Kazuyuki Sugahara; Takako Ishii; Ikuo Yamashina
- Book ID
- 102988690
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 748 KB
- Volume
- 166
- Category
- Article
- ISSN
- 0003-2697
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β¦ Synopsis
A method is described for the assay of sulfotransferases, which transfer sulfate from 3'-phosphoadenosine-5'-phosphosulfate (PAPS) to glycosaminoglycan acceptors. Following the sulfation reactions, the [35S]sulfate-labeled products are precipitated and then separated from a sulfate donor ([35S]PAPS) and its degradation products by a paper disk method, and then the radioactivity remaining on the paper disk is subsequently determined by liquid scintillation counting. The rapidity and simplicity of the method are advantageous for multiple assays and have allowed us to establish assay conditions for serum sulfotransferases which introduce sulfate at position 6 of the internal N-acetylgalactosamine units of chondroitin, position 2 (amino group) of the glucosamine units of heparan sulfate and sugar units of keratan sulfate, respectively. The assay method will be applicable with modification to the assay of other glycosaminoglycan sulfotransferases and glycoprotein sulfotransferases.
π SIMILAR VOLUMES
We have developed a continuous spectrophotometric coupled-enzyme assay for sulfotransferase activity. This assay is based on the regeneration of 3-phosphoadenosine-5-phosphosulfate (PAPS) from the desulfated 3-phosphoadenosine-5-phosphate (PAP) by a recombinant aryl sulfotransferase using p-nitrophe