Author/Authors :
Su، نويسنده , , Dan and Ren، نويسنده , , Xiaojun and You، نويسنده , , Delin and Li، نويسنده , , Dan and Mu، نويسنده , , Ying and Yan، نويسنده , , Ganglin and Zhang، نويسنده , , Yan and Luo، نويسنده , , Yuanming and Xue، نويسنده , , Yan and Shen، نويسنده , , Jiacong and Liu، نويسنده , , Zi and Luo، نويسنده , , Guimin، نويسنده ,
Abstract :
A novel strategy for design of haptens that were used to produce catalytic antibodies was developed and three monoclonal antibodies, 3G5, 2F3, and 5C9, were generated using this strategy. These monoclonal antibodies were converted into selenium-containing abzymes by chemically modifying the hydroxyl group of serines followed by sodium hydrogen selenide displacement. These selenium-containing abzymes exhibited remarkable glutathione peroxidase activity, which surpasses the activity of some native glutathione peroxidases. The activities of the selenium-containing abzymes Se-3G5, Se-2F3, and Se-5C9 which catalyzed reduction of hydroperoxides by glutathione were 2.23, 4.20, and 3.79 times that of rabbit liver glutathione peroxidase, respectively. Detailed steady-state kinetics study on Se-2F3 was carried out and the value of kcat/Km (H2O2) was found to be 2.11 × 107 M−1 min−1 which was supposed to be one of the highest among the known catalytic antibodies. The data of association constants and glutathione peroxidase activities of these catalytic antibodies and the steady-state kinetics of Se-2F3 showed that the method might be a remarkably efficient one for generating catalytic antibodies with glutathione peroxidase activity.
Keywords :
Catalytic antibody , hapten design , Selenium , Glutathione Peroxidase