Urdal D L, Mochizuki D, Conlon P J, March C J, Remerowski M L, Eisenman J, Ramthun C, Gillis S
J Chromatogr. 1984 Jul 27;296:171-9. doi: 10.1016/s0021-9673(01)96410-6.
Reversed-phase high-performance liquid chromatography has been used to purify to homogeneity two different lymphokines. Human IL-2 was purified on a C8 reversed-phase column in pyridine-acetate-propanol followed by chromatography on a C18 reversed-phase column in trifluoroacetic acid-acetonitrile. Protein sequence analysis of in situ-generated cyanogen bromide peptides obtained from this preparation established the homogeneity of this material and confirmed the amino acid sequence predicted from the published DNA sequence. Murine CSF-2 alpha was purified on a C18 reversed-phase column in trifluoroacetic acid-acetonitrile followed by chromatography on the same column in pyridine-acetate-propanol. The final preparation yielded a single band on a sodium dodecyl sulfate-polyacrylamide gel with a molecular weight of 24,500.
反相高效液相色谱法已被用于将两种不同的淋巴因子纯化至同质。人白细胞介素-2在吡啶 - 醋酸盐 - 丙醇体系中的C8反相柱上进行纯化,随后在三氟乙酸 - 乙腈体系中的C18反相柱上进行色谱分离。对从该制剂中获得的原位生成的溴化氰肽进行蛋白质序列分析,确定了该物质的同质性,并证实了从已发表的DNA序列预测的氨基酸序列。小鼠集落刺激因子-2α在三氟乙酸 - 乙腈体系中的C18反相柱上进行纯化,随后在吡啶 - 醋酸盐 - 丙醇体系中的同一柱上进行色谱分离。最终制剂在十二烷基硫酸钠 - 聚丙烯酰胺凝胶上产生一条单一的条带,分子量为24,500。