Institute of Engineering in Life Sciences, Section IV: Biomolecular Separation Science, Karlsruhe Institute of Technology, 76131 Karlsruhe, Germany.
Biotechnol Bioeng. 2011 Nov;108(11):2661-9. doi: 10.1002/bit.23229. Epub 2011 Jul 13.
The application of high throughput experimentation (HTE) in protein purification process development has created an analytical bottleneck. Using a new label-free and non-invasive methodology for analyzing multicomponent protein mixtures by means of spectral measurements, we show that the analytical throughput for selective protein quantification can be increased significantly. An analytical assay based on this new methodology was shown to generate very precise results. Further, the assay was successfully applied as analytics for a resin screening performed in HTE mode. The increase in analytical throughput was obtained without decreasing the level of information when compared to analytical chromatography. This proves its potential as a valuable analytical tool in conjugation with high throughput process development (HTPD). Further, fast selective protein quantification can enhance process control in a commercial production environment and, hence, minimize the need for off-line release analysis.
高通量实验(HTE)在蛋白质纯化工艺开发中的应用造成了分析瓶颈。我们采用一种新的无标记和非侵入性方法,通过光谱测量来分析多组分蛋白质混合物,结果表明,选择性蛋白质定量分析的通量可以显著提高。事实证明,基于这种新方法的分析测定能够产生非常精确的结果。此外,该测定法还成功地用作 HTE 模式下树脂筛选的分析方法。与分析色谱法相比,在不降低信息量的情况下提高了分析通量。这证明了它作为与高通量工艺开发(HTPD)相结合的有价值的分析工具的潜力。此外,快速选择性蛋白质定量可以增强商业生产环境中的过程控制,从而最大限度地减少对离线放行分析的需求。