Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7558241 | Analytical Biochemistry | 2015 | 7 Pages |
Abstract
Sialyltransferases are important enzymes of glycobiology and the related biotechnologies. The development of sialyltransferases calls for access to quick, inexpensive, and robust analytical tools. We have established an assay for simultaneous characterization of sialyltransferase activity, error hydrolysis, and site selectivity. The described assay does not require expensive substrates, is very sensitive (limit of detection = 0.3 μU), and is easy to perform. It is based on sialylation of nitrophenyl galactosides; the products thereof are separated and quantified by ion pair reversed phase high-performance liquid chromatography with ultraviolet detection.
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Tibor Czabany, Katharina Schmölzer, Christiane Luley-Goedl, Doris Ribitsch, Bernd Nidetzky,