Kawasaki H, Suzuki K
Department of Molecular Biology, Tokyo Metropolitan Institute of Medical Science, Japan.
Anal Biochem. 1990 May 1;186(2):264-8. doi: 10.1016/0003-2697(90)90077-m.
Separation of peptides by reversed-phase liquid chromatography is significantly affected by sodium dodecyl sulfate (SDS) in the sample solution. The strongly acidic group of SDS binds to the reversed-phase column where it serves as an ion exchanger and retards the elution of peptides. By using a DEAE precolumn connected in series to a reversed-phase column, the interference of SDS in the separation of peptides by reversed-phase chromatography can be significantly diminished. This simple method is applicable to the separation of peptide mixtures obtained by digestion of proteins extracted from SDS-polyacrylamide gels. Peptide production with some proteases in the presence of SDS was examined using the present method. Lysylendopeptidase was suitable for digestion in the presence of SDS, but V8 protease was not.
样品溶液中的十二烷基硫酸钠(SDS)对反相液相色谱法分离肽段有显著影响。SDS的强酸性基团会与反相柱结合,在柱上起到离子交换剂的作用,从而延缓肽段的洗脱。通过将DEAE预柱与反相柱串联使用,可以显著减少SDS对反相色谱法分离肽段的干扰。这种简单的方法适用于分离从SDS-聚丙烯酰胺凝胶中提取的蛋白质经消化后得到的肽段混合物。使用本方法研究了在SDS存在下一些蛋白酶的肽段生成情况。赖氨酰内肽酶适合在SDS存在下进行消化,但V8蛋白酶不适合。