School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, Geneva, Switzerland.
J Sep Sci. 2010 Aug;33(16):2465-77. doi: 10.1002/jssc.201000023.
The objective of this study was to evaluate various chromatographic approaches for peptide analysis. Initially, the ultra-HPLC (UHPLC) strategy, which consists of using columns packed with sub-2 microm particles at a maximal pressure of 1000 bar, was tested. To limit the backpressure generated by small particles, columns packed with superficially porous sub-3 microm particles (fused-core technology) that should theoretically improve mass transfer, particularly beneficial for large biomolecules, were investigated. To evaluate these claims, kinetic plots were constructed in both isocratic and gradient modes at ambient and elevated temperature (up to 90 degrees C). For peptide analysis, both UHPLC and fused-core technologies showed a significant gain in peak capacity when compared with conventional HPLC using 5 mum particles and monolithic supports. Additionally, it has been shown that high temperature was of utmost interest to further improve kinetic performance and peak shape due to the improvement of secondary interaction kinetics. Finally, the best conditions developed for UHPLC using the gradient kinetic plot methodology were applied to the analysis of a complex tryptic digest of various proteins. The expected and experimental peak capacity values obtained were similar. In addition, the resolving power of UHPLC at 60 degrees C was appropriate for resolving complex mixtures of peptides.
本研究旨在评估各种用于肽分析的色谱方法。首先,测试了超高效液相色谱(UHPLC)策略,该策略包括使用填充有亚 2 微米颗粒的最大压力为 1000 巴的柱子。为了限制小颗粒产生的背压,研究了使用表面多孔亚 3 微米颗粒(熔融核技术)填充的柱子,理论上这种技术可以改善传质,特别是对大分子生物分子有益。为了评估这些说法,在环境和升高的温度(高达 90 摄氏度)下以等度和梯度模式构建了动力学图。对于肽分析,与使用 5 微米颗粒和整体式载体的常规 HPLC 相比,UHPLC 和熔融核技术都显示出显著提高的峰容量。此外,已经表明,由于改善了二次相互作用动力学,高温对于进一步改善动力学性能和峰形非常重要。最后,使用梯度动力学图方法为 UHPLC 开发的最佳条件应用于各种蛋白质的复杂胰蛋白酶消化物的分析。获得的预期和实验峰容量值相似。此外,60°C 时 UHPLC 的分辨率适用于解析复杂的肽混合物。