摘要
建立了重组hepcidin的分离纯化方法,并鉴定其抗菌活性。经金属螯合初步纯化的重组蛋白在cysteine/cystine氧化还原体系中氧化形成二硫键,用变性条件下的凝胶过滤除去多聚体,稀释复性后用于肠激酶酶切反应,得到重组hepcidin。融合蛋白His-hepcidin经氧化、复性后的总收率为50%,纯度大于95%。酶切后所得重组hepcidin经抑菌圈试验检验,对枯草芽孢杆菌具有抗菌活性。LC-ESI-MS与园二色光谱检测显示重组hepcidin与天然hepcidin相对分子质量相同、二级结构相似。
Method of isolation and purification of recombinant hepcidin was described, and the bioactivity of the protein was assayed in this paper. The oxidation of his-hepcidin was carried out in the cysteine-cystine system, and the multimers were removed through gel filtration under denaturation condition. Then the protein was refolded by continuous dilution and digested by enterokinase. The total yield of his-hepcidin before enterokinase cleavage is 50%, and the purity is above 95%. Through agar diffusion assay, the recombinant hepcidin displayed obvious antibacterial activity against B. subtilis. The LC-ESI-MS analysis of recombinant hepcidin showed that the meas- ured molecular weight accorded with the calculated molectilar weight, and the CD spectrum indicated that the secondary structure of recombinant hepeidin is similar with native hepeidin.
出处
《微生物学通报》
CAS
CSCD
北大核心
2006年第4期129-133,共5页
Microbiology China
关键词
重组hepeidin
二硫键
复性
纯化
Recombinant hepeidin, Disulfide bonds, Refolding, Purification
