Hjertén S, Liu Z Q, Zhao S L
J Biochem Biophys Methods. 1983 Feb;7(2):101-13. doi: 10.1016/0165-022x(83)90044-1.
Following electrophoresis or isoelectric focusing in gels of polyacrylamide the protein band of interest is cut out and placed above a sucrose gradient column, containing carrier ampholytes (Pharmalyte). By electrophoresis, isoelectric focusing or displacement electrophoresis the proteins migrate out of the gel slice and into the isoelectric focusing column for concentration and further purification. From this column, the proteins can be withdrawn and their isoelectric points determined. Even after staining with Coomassie Brilliant Blue at least some proteins can be recovered by this technique and used for further analyses, for instance amino acid determinations. The focusing in a pH gradient by carrier ampholytes can be replaced by an electrophoresis in a conductivity gradient column. However, in comparison with isoelectric focusing, this concentration technique has the drawback of not permitting further purification of the eluted protein.
在聚丙烯酰胺凝胶中进行电泳或等电聚焦后,将感兴趣的蛋白条带切下,置于含有载体两性电解质(Pharmalyte)的蔗糖梯度柱上方。通过电泳、等电聚焦或置换电泳,蛋白质从凝胶切片中迁移出来,进入等电聚焦柱进行浓缩和进一步纯化。从该柱中,可以取出蛋白质并测定其等电点。即使在用考马斯亮蓝染色后,至少一些蛋白质也可以通过该技术回收并用于进一步分析,例如氨基酸测定。通过载体两性电解质在pH梯度中的聚焦可以被在导电率梯度柱中的电泳所取代。然而,与等电聚焦相比,这种浓缩技术的缺点是不允许对洗脱的蛋白质进行进一步纯化。