Glutathione transferase activity with a novel substrate mimics the activation of the prodrug azathioprine

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• 作者：Sanela Kurtovic ; Leif Grehn ; Andreas Karlsson ; Ulf Hellman ; Bengt Mannervik
• 关键词：Azathioprine ; Enzyme assay ; GST ; Prodrug mimetic
• 刊名：Analytical Biochemistry
• 出版年：2008
• 出版时间：15 April 2008
• 年：2008
• 卷：375
• 期：2
• 页码：339-344
• 全文大小：138 K

文摘

Azathioprine is a prodrug that is widely used clinically as an immunosuppressive agent. The pharmacological action of azathioprine is associated with the release of 6-mercaptopurine by a reaction involving glutathione. This biotransformation of azathioprine is catalyzed by glutathione transferases (GSTs). The nonenzymatic reaction with glutathione is minimal in comparison with the GST-catalyzed process, but azathioprine is still a slow substrate in comparison with the most effective GST substrates. Novel GSTs with higher catalytic efficiency toward azathioprine could be useful in novel therapeutic applications; therefore, directed evolution of GSTs for enhanced activities is desirable. However, screening for variants having higher catalytic activity with azathioprine is a time-consuming process due to the low activity with this substrate. A new chromogenic and faster substrate, 1-methyl-4-nitro-5-(4-nitrophenylthio)-1H-imidazole (NPTI), has been synthesized and characterized by assays with several GSTs. The novel substrate mimicked azathioprine in the reaction with glutathione catalyzed by alpha class GSTs and, therefore, is a valuable surrogate in the screening of large mutant libraries. NPTI may also find use in the elucidation of the exact mechanism of immunosuppression effected by azathioprine where there is evidence that the imidazole moiety of azathioprine, rather than 6-mercaptopurine, is involved.