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采用核壳型硅胶颗粒的用于蛋白质组学应用的快速高效液相色谱分离。

Fast high performance liquid chromatography separations for proteomic applications using Fused-Core® silica particles.

机构信息

Advanced Materials Technology Inc., 3521 Silverside Rd., Quillen Bldg, Wilmington, DE 19810, USA.

出版信息

J Chromatogr A. 2012 Mar 9;1228:232-41. doi: 10.1016/j.chroma.2011.07.082. Epub 2011 Jul 30.

Abstract

The separation range of superficially porous particles (Fused-Core®) has been extended by design of particles with 160 Å pores. These particles show superior kinetics (lower resistance to mass transfer), allowing fast separations of peptides and small proteins (molecular weights of <15,000). The high efficiency and relatively low back pressure of these 2.7 μm Fused-Core particles has been maintained so that separations can be performed with conventional HPLC instruments. Longer columns can be used for higher resolution of complex mixtures of peptides, such as proteolytic digests. Highly reproducible separations of peptides at elevated temperatures with low pH mobile phases are maintained as a result of a stable bonded stationary phase. The utility of such highly stable materials is exemplified by separations of problematic amyloid peptides at low pH (TFA mobile phase) at an operational temperature of 100 °C. To address the issue of poor peptide peak shape in formic acid-containing mobile phases we show that the addition of 10-20 mM ammonium formate improves peak shape, retention and load tolerance of peptides. Use of the Fused-Core particle materials for separations of synthetic peptides and tryptic digests yields peak capacities that are comparable to those obtained using columns packed with sub-2-μm particles, but with less than one-half of the operating back pressure. A peak capacity of 530 was obtained in 150 min on coupled columns of HALO Peptide ES-C18 with a combined length of 250 mm.

摘要

通过设计具有 160Å 孔径的颗粒,扩展了表面多孔颗粒(Fused-Core®)的分离范围。这些颗粒显示出优异的动力学性能(传质阻力更低),允许快速分离肽和小蛋白质(分子量小于 15000)。这些 2.7μm 的 Fused-Core 颗粒保持了高效率和相对较低的背压,因此可以在常规 HPLC 仪器上进行分离。更长的柱子可以用于分离肽的复杂混合物,如蛋白酶解产物,以获得更高的分辨率。由于稳定的键合固定相,在低 pH 流动相和升高的温度下可以保持对肽的高度重现性分离。由于这种高度稳定的材料的实用性,我们通过在 100°C 的操作温度下在低 pH(TFA 流动相)下分离有问题的淀粉样肽来举例说明。为了解决在含有甲酸的流动相中肽峰形状不佳的问题,我们表明添加 10-20mM 甲酸铵可以改善肽的峰形、保留和负载耐受性。使用 Fused-Core 颗粒材料进行合成肽和胰蛋白酶消化物的分离,可获得与使用填充有亚 2μm 颗粒的柱子相当的峰容量,但操作背压不到一半。在耦合的 HALO Peptide ES-C18 柱上,在 150 分钟内获得了 530 的峰容量,总长度为 250mm。

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