Ma Y, Ito Y
Laboratory of Biophysical Chemistry, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892 1676, USA.
J Chromatogr A. 1997 May 30;771(1-2):81-8. doi: 10.1016/s0021-9673(97)00065-4.
Peptides without protecting groups have been successfully separated by pH-zone-refining countercurrent chromatography (CCC) using an ion-pair reagent, di-(2-ethylhexyl)phosphoric acid (DEHPA), as a modifier in the stationary phase. Preliminary studies indicated that two parameters, i.e., the DEHPA concentration in the stationary phase and hydrophobicity of the solvent system should be adjusted according to the hydrophobicity of the analytes. Hydrophobic and hydrophilic groups of dipeptides were each separated under optimized conditions. The method was successfully applied to gram-quantity separations of bacitracin complex and bovine insulin.
使用离子对试剂二(2-乙基己基)磷酸(DEHPA)作为固定相改性剂,通过pH区带精制逆流色谱(CCC)成功分离了无保护基团的肽。初步研究表明,应根据分析物的疏水性调整两个参数,即固定相中DEHPA的浓度和溶剂系统的疏水性。在优化条件下分别分离了二肽的疏水基团和亲水基团。该方法成功应用于杆菌肽复合物和牛胰岛素的克级分离。