摘要
目的:建立重组人B淋巴细胞刺激因子受体-抗体融合蛋白(TACI-Fc)的肽图分析方法。方法:将TACI-Fc蛋白用胰蛋白酶酶解、用尿素将蛋白分子变性、用二硫苏糖醇打断二硫键、用碘乙酰胺封闭巯基、用胰蛋白酶再次酶解等方法处理后,采用高效液相色谱分析,色谱柱为Vydac C18(250 mm×4.6 mm,5μm),流动相A液为含0.1%三氟乙酸的水溶液,流动相B液为含0.1%三氟乙酸的乙腈溶液,梯度洗脱,流速为1.0 mL.min-1,检测波长为214 nm。结果:TACI-Fc蛋白被有效酶解,酶解后的各个片段能够很好的分离。结论:本法准确性高,重复性好,是重组人B淋巴细胞刺激因子受体-抗体融合蛋白结构确认的有效方法。
Objective：To establish a peptide mapping analysis method in recombinant human B lymphocyte stimulator receptor：IgG Fc fusion protein.Method：The TACI-Fc protein was digested with trypsin and then was denatured by urea.Next,the disulfide bonds were interrupted by dithiothreitol and the thiol groups were closed with iodoacetamide.Finally,the treated TACI-Fc protein was digested with trypsin again and assayed by HPLC.Vydac C18（250 mm×4.6 mm,5 μm） was used as analysis column,0.1% trifluoroacetic acid in water and 0.1% trifluoroacetic acid in acetonitrile were used as mobile phase A and mobile phase B,respectively.The gradient elution process was performed.The detection wavelength was 214 nm and flow rate was 1.0 mL·min-1.Results：The fragments of TACI-Fc were well digested and separated.Conclusion：This method is accurate,stable,and reliable for testing of human B lymphocyte stimulator receptor：IgG Fc fusion protein peptide mapping.
出处
《药物分析杂志》
CAS
CSCD
北大核心
2011年第6期1185-1187,共3页
Chinese Journal of Pharmaceutical Analysis
关键词
重组
淋巴细胞
刺激因子
受体
抗体
融合蛋白
肽图
recombinant
lymphocyte
stimulator
receptor
antibody
fusion protein
peptide mapping
