Yoshida T
Scientific Instrument Division, Tosoh Corporation, Tokyo Research Center, Kanagawa-ken, Japan.
Anal Chem. 1997 Aug 1;69(15):3038-43. doi: 10.1021/ac9702204.
A new method is established for separating peptides in normal phase liquid chromatography using TSK gel Amide-80, carbamoyl groups bonded to a silica gel matrix, and an acetonitrile-water solution containing 0.1% trifluoroacetic acid. Peptide retention time increased with acetonitrile concentration in the initial eluent. Hydrophilic peptides with no retention in a reversed phase column were retained and separated in the present method. Separation selectivities in the present and reversed phase methods differed significantly. Two-dimensional separation of protein digest using reversed and normal phases was conducted, taking advantage of the differences in selectivities. All peptides obtained from the digest could be separated completely. The present method is useful for separating peptide mixtures in conjunction with reversed phase liquid chromatography. Peptide recovery from the Amide-80 column exceeded 80%, as with the reversed phase column, and repeatability and reproducibility were satisfactory.
建立了一种新方法,用于在正相液相色谱中使用TSK凝胶酰胺-80(键合在硅胶基质上的氨基甲酰基)和含有0.1%三氟乙酸的乙腈-水溶液分离肽段。肽段的保留时间随初始洗脱液中乙腈浓度的增加而延长。在反相柱中无保留的亲水性肽段在本方法中得以保留和分离。本方法与反相方法的分离选择性有显著差异。利用选择性差异,对蛋白质消化产物进行了反相和正相二维分离。消化产物得到的所有肽段都能完全分离。本方法可与反相液相色谱结合用于分离肽混合物。与反相柱一样,从酰胺-80柱上回收肽段的回收率超过80%,重复性和重现性令人满意。