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毛细管电泳-质谱联用技术在生物样品氨基酸分析中的新进展

New Advances in Amino Acid Profiling in Biological Samples by Capillary Electrophoresis-Mass Spectrometry.

作者信息

Shanmuganathan Meera, Britz-McKibbin Philip

机构信息

Department of Chemistry and Chemical Biology, McMaster University, Hamilton, ON, Canada.

出版信息

Methods Mol Biol. 2019;2030:327-350. doi: 10.1007/978-1-4939-9639-1_25.

Abstract

Capillary electrophoresis-mass spectrometry (CE-MS) offers a high efficiency microseparation platform for amino acid profiling when analyzing volume-restricted biological samples, such as a dried blood spot punch. Direct analysis of amino acids and their analogs is routinely achieved using strongly acidic buffer conditions under positive-ion mode detection with a coaxial sheath liquid interface for electrospray ionization (ESI). New advances in online sample preconcentration, pre-column chemical derivatization, and/or low flow/sheathless CE-MS interface designs can further improve sensitivity while allowing for resolution of amino acid stereoisomers and labile aminothiols with low nanomolar detection limits. Additionally, multiplexed separations in CE-MS based on serial injection of seven or more samples within a single run greatly boosts sample throughput (<2-3 min/sample) without added infrastructure costs while allowing for stringent quality control and signal batch correction. Accurate prediction of the electromigration behavior of amino acids and their analogs offers a convenient approach for structural elucidation that is complementary to high-resolution MS and MS/MS. Simultaneous analysis of amino acids together with other classes of ionic metabolites by CE-MS allows for comprehensive metabolomic screening as required for new advances in clinical medicine, nutritional sciences, and population health.

摘要

毛细管电泳-质谱联用(CE-MS)在分析体积受限的生物样本(如干血斑冲孔样本)时,为氨基酸谱分析提供了一个高效的微分离平台。在正离子模式检测下,使用强酸性缓冲条件并结合用于电喷雾电离(ESI)的同轴鞘液接口,可常规实现对氨基酸及其类似物的直接分析。在线样品预浓缩、柱前化学衍生和/或低流量/无鞘CE-MS接口设计方面的新进展,可进一步提高灵敏度,同时实现氨基酸立体异构体和具有低纳摩尔检测限的不稳定氨基硫醇的分离。此外,基于在单次运行中连续进样七个或更多样品的CE-MS多重分离,在不增加基础设施成本的情况下,极大地提高了样品通量(<2-3分钟/样品),同时允许进行严格的质量控制和信号批次校正。准确预测氨基酸及其类似物的电迁移行为,为结构解析提供了一种便捷方法,它是对高分辨率质谱和串联质谱的补充。通过CE-MS同时分析氨基酸和其他类别的离子代谢物,可实现临床医学、营养科学和人群健康新进展所需的全面代谢组学筛查。

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