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Capillary Isotachophoresis-Nanoelectrospray Ionization-Selected Reaction Monitoring MS via a Novel Sheathless Interface for High Sensitivity Sample Quantification

机译:毛细管等速电泳-纳米电喷雾电离选择反应监测系统,通过新型无鞘接口实现高灵敏度样品定量

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A novel sheathless capillary isotachophoresis (CITP/CZE)-mass spectrometry (MS) interface featuring a large inner diameter (i.d.) separation capillary, and a detachable small i.d. porous electrospray ionization (ESI) emitter was developed in this study to simultaneously achieve large sample loading capacity and stable nanoESI operation. Crucial operating parameters, including sample loading volume, flow rate, and separation window, were systematically investigated to attain optimum CITP/CZE separation efficiency and MS detection sensitivity. The performance of CITP/CZE-nanoESI-MS using the new sheathless interface was evaluated for its achievable low limit of quantification (LOQ) by analyzing targeted peptides, leu-enkephalin and angiotensin II, spiked in a BSA tryptic digest matrix at different concentrations. A linear dynamic range spanning 4.5 orders of magnitude and a 10 pM LOQ with measurement reproducibility of the CV < 22% were obtained experimentally for both targeted peptides, representing a 5-fold sensitivity improvement as compared to using the sheath liquid interface developed previously.
机译:一种新颖的无鞘毛细管等速电泳(CITP / CZE)-质谱(MS)界面,具有大内径(i.d.)分离毛细管和可分离的小i.d.这项研究中开发了多孔电喷雾电离(ESI)发射器,以同时实现大样品加载容量和稳定的nanoESI操作。为了获得最佳的CITP / CZE分离效率和MS检测灵敏度,系统地研究了关键的操作参数,包括样品上样量,流速和分离窗口。通过分析掺入BSA胰蛋白酶消化基质中不同浓度的目标肽,亮氨酸-脑啡肽和血管紧张素II,评估了使用新型无鞘界面的CITP / CZE-nanoESI-MS的性能可实现的低定量下限(LOQ)。通过实验获得了两种目标肽的线性动态范围,跨度为4.5个数量级,测量重现性CV <22%,LOP为10 pM,与使用先前开发的鞘液界面相比,灵敏度提高了5倍。

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