Institute of Engineering in Life Sciences, Section IV: Biomolecular Separation Engineering, Karlsruhe Institute of Technology, Karlsruhe, Germany.
J Chromatogr A. 2013 Apr 12;1285:78-87. doi: 10.1016/j.chroma.2013.02.017. Epub 2013 Feb 14.
pH gradient protein separations are widely used techniques in the field of protein analytics, of which isoelectric focusing is the most well known application. The chromatographic variant, based on the formation of pH gradients in ion exchange columns is only rarely applied due to the difficulties to form controllable, linear pH gradients over a broad pH range. This work describes a method for the systematic generation of buffer compositions with linear titration curves, resulting in well controllable pH gradients. To generate buffer compositions with linear titration curves an in silico method was successfully developed. With this tool, buffer compositions for pH gradient ion exchange chromatography with pH ranges spanning up to 7.5 pH units were established and successfully validated. Subsequently, the buffer systems were used to characterize the elution behavior of 22 different model proteins in cation and anion exchange pH gradient chromatography. The results of both chromatographic modes as well as isoelectric focusing were compared to describe differences in between the methods.
pH 梯度蛋白分离技术在蛋白质分析领域得到了广泛应用,其中等电聚焦是最著名的应用。基于离子交换柱中 pH 梯度形成的色谱变体由于难以在较宽的 pH 范围内形成可控的线性 pH 梯度,因此很少应用。本工作描述了一种系统产生具有线性滴定曲线的缓冲组成的方法,从而产生可良好控制的 pH 梯度。为了生成具有线性滴定曲线的缓冲组成,成功开发了一种计算机模拟方法。使用此工具,建立了 pH 范围跨越至 7.5 pH 单位的 pH 梯度离子交换色谱的缓冲组成,并对其进行了成功验证。随后,使用缓冲系统对 22 种不同的模型蛋白质在阳离子和阴离子交换 pH 梯度色谱中的洗脱行为进行了表征。对两种色谱模式以及等电聚焦的结果进行了比较,以描述这些方法之间的差异。