PLLA-PCys co-electrospun fibers for capture and elution of glutathione S-transferase

被引:7
作者
Lu TianCheng [1 ,2 ,3 ]
Sun Jing [1 ,3 ]
Dong XiaoQing [1 ,3 ]
Chen XueSi [1 ]
Wang Yu [1 ]
Jing XiaBin [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Jilin Agr Univ, Inst Life Sci, Changchun 130118, Peoples R China
[3] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
来源
SCIENCE IN CHINA SERIES B-CHEMISTRY | 2009年 / 52卷 / 12期
基金
中国国家自然科学基金;
关键词
electrospun fibers; glutathione; glutathione S-transferase; protein separation and purification; PROTEINS; PRODUCT;
D O I
10.1007/s11426-009-0291-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The copolymer poly(L-lactic acid)-b-poly(L-cysteine) (PLA-b-PCys) was co-electrospun with PLGA into ultrafine fibers. The reduced glutathione (GSH) was conjugated to the fiber surfaces via disulfide bonds. The glutathione S-transferase (GST) was captured onto the GSH fibers via specific substrate-enzyme interaction between the bound GSH and GST. The captured GST was eluted with free GSH aqueous solution and lyophilized to get pure GST powders. The results show that the GSH moieties on the fiber surface retain the bioactivity of the free GSH and thus they can bind specifically with GST and the GST in solution is captured onto the fiber surface. In addition, the bound GSH is not as active as free GSH so that the captured GST can be eluted off from the fiber by free GSH aqueous solution. Based on this principle, GST itself or its fused proteins can be separated and purified very easily. The preliminary purification efficiency is 6.5 mg center dot(g(PCys))(-1). Further improvements are undertaken.
引用
收藏
页码:2033 / 2037
页数:5
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