| Autor: |
Wang J; Key Laboratory of Fermentation Engineering (Ministry of Education) & National '111' Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan 430068, Hubei, China.; Key Laboratory of Tumor Microenvironment and Immunotherapy, Medicsl School of China Three Gorges University, Yichang 443002, Hubei, China., Liu X; Key Laboratory of Fermentation Engineering (Ministry of Education) & National '111' Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan 430068, Hubei, China., Ma H; Key Laboratory of Fermentation Engineering (Ministry of Education) & National '111' Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan 430068, Hubei, China.; Key Laboratory of Tumor Microenvironment and Immunotherapy, Medicsl School of China Three Gorges University, Yichang 443002, Hubei, China., Chen Q; Key Laboratory of Fermentation Engineering (Ministry of Education) & National '111' Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan 430068, Hubei, China., Liu S; Key Laboratory of Fermentation Engineering (Ministry of Education) & National '111' Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan 430068, Hubei, China.; Key Laboratory of Tumor Microenvironment and Immunotherapy, Medicsl School of China Three Gorges University, Yichang 443002, Hubei, China. |
| Abstrakt: |
Ornithine decarboxylase (ODC) is a key enzyme in the biosynthetic pathway of polyamines and catalyzes the decarboxylation of ornithine to produce putrescine. Inhibition of ODC activity is a potential approach for the prevention and treatment of many diseases including cancer, as the expression levels and the activities of ODC in many abnormal cells and tumor cells are generally higher than those of normal cells. The discovery and evaluation of ODC inhibitors rely on the monitoring of the reaction processes catalyzed by ODC. There are several commonly used methods for analyzing the activity of ODC, such as measuring the yield of putrescine by high performance liquid chromatography, or quantifying the yield of isotope labelled carbon dioxide. However, the cumbersome operation and cost of these assays, as well as the difficulty to achieve high-throughput and real-time detection, hampered their applications. In this work, we optimized a real-time label-free method for analyzing the activity of ODC based on the macromolecule cucurbit[6]uril (CB6) and a fluorescent dye, DSMI (trans-4-[4-(dimethylamino) styryl]-1-methylpyridinium iodide). Finally, the optimized method was used to determine the activities of different ODC inhibitors with different inhibition mechanisms. |
