首页 | 本学科首页   官方微博 | 高级检索  
     检索      

反相高效液相色谱法分离蛋白质的研究
引用本文:张华,王俊德,钟虹敏,罗丽梅.反相高效液相色谱法分离蛋白质的研究[J].色谱,1998,16(3):220-222.
作者姓名:张华  王俊德  钟虹敏  罗丽梅
作者单位:大连理工大学染料、表面活性剂精细化工国家重点实验室,中国科学院大连化学物理研究所
摘    要:采用反相高效液相色谱法考察了几种大孔硅胶烷基键合固定相在等度淋洗条件下进行蛋白质分离的色谱性能。研究了冲洗剂中有机溶剂异丙醇的浓度、离子对酸(TFA)浓度对蛋白质保留时间的影响。探讨了蛋白质在RP-HPLC中的保留机理。结果表明,大孔硅胶(20~30nm)短链(C4和C8)烷基键合固定相适合蛋白质的分离。

关 键 词:大孔硅胶烷基键合固定相  蛋白质分离  反相高效液相色谱法  

Study of Protein Separation by Reversed Phase High Performance Liquid Chromatography
H Zhang,J Wang,H Zhong,L Luo.Study of Protein Separation by Reversed Phase High Performance Liquid Chromatography[J].Chinese Journal of Chromatography,1998,16(3):220-222.
Authors:H Zhang  J Wang  H Zhong  L Luo
Institution:State Key Laboratory of Dye and Surfactant Fine Chemicals, Dalian University of Technology, Dalian, 116012.
Abstract:Reversed-phase high performance liquid chromatography (RP-HPLC) of protein on large pore silica (20-30 nm) n-alkyl-bonded(C4 and C5) phase columns was studied using a trifluoroacetic acid (TFA)/2-propanol mobile phase system. The influence of concentration of organic modifier (2-propanol) and ion-pairing acid (TFA) on the protein retention time was examined. The results showed that the plot of the retention time vs-2-propanol concentration in mobile phase was U-shaped. The mechanism of protein in reversed-phase high performance liquid chromatography is also discussed.
Keywords:reversed phase high performance liquid chromatography  separation of protien  large pore silica alkyl bonded phase  
本文献已被 CNKI 维普 等数据库收录!
点击此处可从《色谱》浏览原始摘要信息
点击此处可从《色谱》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号