Irvine G B
Department of Biochemistry, Queen's University of Belfast, U.K.
J Chromatogr. 1987 Aug 28;404(1):215-22. doi: 10.1016/s0021-9673(01)86851-5.
Polypeptides subjected to high-performance liquid chromatography on a TSK G2000SW column in acidic mobile phases of low ionic strength underwent a combination of size exclusion and ion exclusion from the matrix. The distribution coefficient (Kd) of each polypeptide was dependent upon the concentration of ion-pairing agent present and increased as the concentration of ion-pairing agent increased. The fractionation range of the column could thus be manipulated by altering the concentration of acid in the mobile phase. The nature of the ion-pairing acid, in terms of hydrophilic or hydrophobic ion pairing, also had an effect on the chromatography, such that hydrophobic ion-pairing agents lead to increased Kd values, especially in the case of the most basic polypeptides. To account for these results it is proposed that the TSK GSW matrix is cationic at low pH, and that ion pairing suppresses the ion exclusion experienced by cationic polypeptides under these conditions.
在低离子强度的酸性流动相中,于TSK G2000SW柱上进行高效液相色谱分析的多肽,经历了基质的尺寸排阻和离子排阻的联合作用。每种多肽的分配系数(Kd)取决于存在的离子对试剂的浓度,并随着离子对试剂浓度的增加而增大。因此,通过改变流动相中酸的浓度,可以操控该柱的分级分离范围。就亲水或疏水离子对而言,离子对酸的性质也对色谱分析有影响,使得疏水离子对试剂导致Kd值增加,尤其是在最碱性的多肽的情况下。为了解释这些结果,有人提出TSK GSW基质在低pH下呈阳离子性,并且在这些条件下离子对抑制了阳离子多肽所经历的离子排阻。