Lindenburg Petrus W, Seitzinger Remco, Tempels F W Alexander, Tjaden Ubbo R, van der Greef Jan, Hankemeier Thomas
Division of Analytical Biosciences, Leiden/Amsterdam Center for Drug Research, Leiden University, The Netherlands.
Electrophoresis. 2010 Dec;31(23-24):3903-12. doi: 10.1002/elps.201000347.
In this research paper, we show that capillary electroextraction (cEE) is capable of fast online peptide concentration and that it can be coupled online to LC-MS to result in a fast and sensitive method. Electroextraction takes place when an electrical field is applied in a two-phase liquid-liquid system. Sample molecules in the organic phase migrate very fast into the aqueous phase and are concentrated in a small zone. In this work, cEE of peptides is developed and coupled online to LC-MS via a switching valve. Comparison of 10 min of cEE-LC-MS with a normal LC-MS injection showed more than 100-fold increased peak heights. Of five model peptides, good calibration curves in the range of 0.05-5 μmol/L were obtained. The linearity was good (R(2) values between 0.984 and 0.996) and RSD between 5% at the highest to 25% at the lowest concentration (n=3). The LOD of bradykinin, angiotensin I-converting enzyme inhibitor and angiotensin I was in the low nmol/L range. Analysis of a tryptic digest of eight model proteins resulted in more than 170 peptides, without bias for pI or hydrophilicity. Urine analysis is demonstrated, resulting in an LOD around 0.04 μmol/L urine for tryptic cytochrome C peptides spiked to urine and an increase of 42% in the number of chromatographic peaks compared with the conventional LC-MS. In summary, cEE-LC-MS is a fast electrophoresis-driven sample preconcentration technique that is quantitative, able to extract a wide peptide range and applicable to bioanalysis.
在本研究论文中,我们表明毛细管电萃取(cEE)能够实现快速在线肽浓缩,并且可以在线与液相色谱-质谱联用,从而形成一种快速且灵敏的方法。当在两相液-液系统中施加电场时,电萃取过程就会发生。有机相中的样品分子会非常快速地迁移到水相中,并浓缩在一个小区域内。在这项工作中,开发了肽的cEE方法,并通过切换阀将其在线与液相色谱-质谱联用。将10分钟的cEE-液相色谱-质谱与常规液相色谱-质谱进样进行比较,结果表明峰高增加了100多倍。对于五种模型肽,在0.05 - 5 μmol/L范围内获得了良好的校准曲线。线性良好(R(2)值在0.984至0.996之间),相对标准偏差在最高浓度时为5%,最低浓度时为25%(n = 3)。缓激肽、血管紧张素I转换酶抑制剂和血管紧张素I的检测限在低纳摩尔/升范围内。对八种模型蛋白质的胰蛋白酶消化产物进行分析,得到了170多种肽,对肽的等电点或亲水性没有偏向性。展示了尿液分析结果,对于添加到尿液中的胰蛋白酶细胞色素C肽,尿液检测限约为0.04 μmol/L,与传统液相色谱-质谱相比,色谱峰数量增加了42%。总之,cEE-液相色谱-质谱是一种快速的电泳驱动样品预浓缩技术,具有定量能力,能够提取广泛的肽范围,适用于生物分析。