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Simultaneous Separation of Cationic and Anionic Proteins Using Zwitterionic Surfactants in Capillary Electrophoresis

机译:两性离子表面活性剂在毛细管电泳中同时分离阳离子和阴离子蛋白

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The zwitterionic surfactant Rewoteric AM CAS U forms a dynamic wall coating that prevents the adsorption of cationic proteins as well as suppresses the electroosmotic flow (EOF). Addition of polarizable anions to buffers containing this zwitterionic surfactant increases the once suppressed EOF to values nearing +3×10~(-4) cm~(2)/(V s). The retention of the EOF allows for the separation of analytes of widely different mobilities and is demonstrated by the simultaneous separation of cationic and anionic proteins. Using a buffer containing optimal amounts of the polarizable anion perchlorate and surfactant CAS U, the proteins lysozyme, ribonuclease A, α-chymotrypsinogen A, and myoglobin are separated in less than 15 min. Efficiencies as high as 1.5 million plates/m and recoveries greater than 91% are observed for proteins injected in distilled water. Migration time reproducibility is ~1% RSD within 1 day and ~3% RSD from day to day. The anionic and cationic proteins can be separated over a pH range of 5.5-9, all yielding good efficiencies.
机译:两性离子表面活性剂Rewoteric AM CAS U形成动态壁涂层,可防止阳离子蛋白质的吸附并抑制电渗流(EOF)。向含有这种两性离子表面活性剂的缓冲液中添加可极化的阴离子会使曾经被抑制的EOF值增加到接近+ 3×10〜(-4)cm〜(2)/(V s)。 EOF的保留可分离出流动性差异很大的分析物,并通过同时分离阳离子和阴离子蛋白得到证明。使用包含最佳量的可极化阴离子高氯酸根和表面活性剂CAS U的缓冲液,可在不到15分钟的时间内分离出溶菌酶,核糖核酸酶A,α-胰凝乳蛋白酶原A和肌红蛋白。对于注入蒸馏水中的蛋白质,观察到的效率高达150万个板/米,回收率大于91%。迁移时间的可重复性在1天内RSD约为1%,每天RSD约为3%。阴离子蛋白和阳离子蛋白可以在5.5-9的pH范围内分离,均产生良好的效率。

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