Institute of Analytical Chemistry of the CAS, Veveří 97, 602 00 Brno, Czech Republic.
Institute of Analytical Chemistry of the CAS, Veveří 97, 602 00 Brno, Czech Republic.
Food Chem. 2022 May 30;377:131986. doi: 10.1016/j.foodchem.2021.131986. Epub 2022 Jan 3.
A method for on-line concentration of milk proteins from large sample volumes using combination of transient isotachophoresis (tITP) and micellar electrokinetic chromatography (MEKC) in fused silica capillary with an inner roughened part has been developed. The method utilizes reversible dynamic adsorption of proteins onto a thin layer of PEG 4000 on the roughened surface of the capillary. In addition, the tITP/MEKC method was combined with capillary isoelectric focusing (CIEF) for on-line concentration, separation, identification and sensitive determination of proteins in skimmed milk. The method allows analysis of up to 50 μL of sample. This study has focused on the four important whey proteins, bovine serum albumin (BSA), α-lactalbumin (α-LA), and two genetic variants of β-lactoglobulin (β-LG A and β-LG B). The proteins were identified on the basis of their migration times and characteristic pI values. The pI values of BSA, α-LA, β-LG A, and β-LG B were determined as 4.7, 4.4, 5.1, and 5.2, respectively. Limits of detection for BSA, α-LA and both β-LG variants were found as 1.2, 1.0 and 1.0 pg mL, respectively. The linearity of calibration curves was characterized by the R = 0.9982. The method provided highly reproducible results as the relative standard deviations of the migration times and peak areas of the examined proteins did not exceed 1.6%.
已经开发出一种使用瞬态等速电泳(tITP)和胶束电动色谱(MEKC)在带有内粗糙部分的熔融石英毛细管中结合对大体积样品中的牛奶蛋白进行在线浓缩的方法。该方法利用蛋白质在毛细管粗糙表面上的 PEG 4000 薄层上的可逆动态吸附。此外,tITP/MEKC 方法与毛细管等电聚焦(CIEF)相结合,用于在线浓缩、分离、鉴定和检测脱脂乳中的蛋白质。该方法允许分析多达 50 μL 的样品。本研究集中于四种重要的乳清蛋白,牛血清白蛋白(BSA)、α-乳白蛋白(α-LA)和两种β-乳球蛋白(β-LG A 和 β-LG B)的遗传变异体。根据它们的迁移时间和特征 pI 值对蛋白质进行鉴定。BSA、α-LA、β-LG A 和 β-LG B 的 pI 值分别确定为 4.7、4.4、5.1 和 5.2。BSA、α-LA 和两种β-LG 变异体的检测限分别为 1.2、1.0 和 1.0 pg mL。校准曲线的线性关系由 R = 0.9982 表示。该方法提供了高度可重现的结果,因为所检查蛋白质的迁移时间和峰面积的相对标准偏差不超过 1.6%。