Institute of Engineering in Life Sciences, Section IV Biomolecular Separation Engineering, Karlsruhe Institute of Technology-KIT, 76131 Karlsruhe, Germany.
J Chromatogr A. 2012 Sep 28;1257:41-7. doi: 10.1016/j.chroma.2012.07.089. Epub 2012 Aug 3.
Size exclusion chromatography (SEC) is often applied for characterization of protein-polyethylene glycol (PEG) conjugates regarding the number of attached PEG chains (PEGamers). SEC analysis is advantageous as it is precise, robust, and straightforward to establish. However, most SEC based assays have a maximal throughput of a few samples per hour. We present a strategy to increase analytical throughput based on combining a short column with a fast flow rate, and finally multivariate calibration in order to compensate for the resolution lost in the trade off for speed. Different multivariate approaches were compared and multilinear regression was shown to result in the most precise calibrations. Further, a dynamic calibration approach was developed in order to account for changes in column performance over time. In this way, it was possible to establish a highly precise assay for protein PEGamer quantification with a throughput of 30 samples per hour.
尺寸排阻色谱法(SEC)常用于分析蛋白质-聚乙二醇(PEG)缀合物的 PEG 链数目(PEGamers)。SEC 分析具有精确、稳健和易于建立的优点。然而,大多数基于 SEC 的测定方法每小时的最大吞吐量为几个样本。我们提出了一种基于短柱与快速流速相结合的策略,以及最终的多元校准,以补偿因速度而导致的分辨率损失。比较了不同的多元方法,结果表明多线性回归可得到最精确的校准。此外,还开发了一种动态校准方法,以补偿柱子性能随时间的变化。通过这种方式,可以建立一种具有 30 个样本/小时的高通量、高度精确的蛋白质 PEGamer 定量分析方法。