화학공학소재연구정보센터
Biotechnology Letters, Vol.38, No.5, 801-807, 2016
Production of a therapeutic protein by fusing it with two fragments of the carboxyl-terminal peptide of human chorionic gonadotropin beta-subunit in Pichia pastoris
Objective To produce a therapeutic protein (endostatin) by fusion with two fragments of the carboxyl-terminal peptide (CTP) of the human chorionic gonadotropin beta-subunit in Pichia pastoris. Results Two CTP sequences were fused to the C-terminal of human endostatin, and the fusion protein (endo-CTP) was expressed by P. pastoris. Endo-CTP inhibited proliferation of endothelial cells with an IC50 of 7 mu g ml(-1), and 30 % of cells were annexin V-positive after treatment with 20 mu g endo-CTP ml(-1) for 48 h. Migration of endothelial cells was inhibited by endo-CTP in a concentration-dependent manner. The half-life of endo-CTP in Sprague-Dawley rats was much longer than that of its commercial counterpart (Endostar). Conclusion A long-acting endostatin can be produced using CTP technology.