摘要
重组人粒细胞集落刺激因子(rhG-CSF)经大肠杆菌温度诱导表达后,其表达产物以包涵体形式存在,包涵体经过变性、复性和分离纯化等步骤处理后得到纯化的rhG-CSF。在一定的实验条件下用单甲氧基聚乙二醇活性酯(mPEG20k-NHS)对rhG-CSF进行化学修饰,所得修饰产物经分离纯化后获得PEG20K-rhG-CSF偶联物。与修饰前的rhG-CSF相比较,尽管修饰后的rhG-CSF体外生物学活性下降至修饰前的20%左右,但其在体内的作用时间能够得到显著的延长,药效有了明显提高。
Recombinant human granulocyte colony-stimulating factor(rhG-CSF) expressed in Escherichia coli in form of inclusion body was modified by monomethoxy polythylene glycol (mPEG20k-NHS) after denaturation, renaturation and purification. The modified rhG-CSF(PEG20k-rhG-CSF) was obtained by purification of modified product. Compared with unmodified rhG-CSF, the modified rhG-CSF had 20% biologic activity of unmodified rhG-CSF in vitro, but it had significantly prolonged action time in vivo with obviously elevating pharmacodynamics.
出处
《生物学杂志》
CAS
CSCD
2008年第2期36-39,共4页
Journal of Biology