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鞘液免费毛细管电泳-质谱联用在有限样本量代谢组学中的应用。

Utility of sheathless capillary electrophoresis-mass spectrometry for metabolic profiling of limited sample amounts.

机构信息

Biomedical Microscale Analytics, Division of Systems Biomedicine and Pharmacology, Leiden Academic Center for Drug Research, Leiden University, the Netherlands.

Biomedical Microscale Analytics, Division of Systems Biomedicine and Pharmacology, Leiden Academic Center for Drug Research, Leiden University, the Netherlands; Netherlands Metabolomics Centre, Leiden, the Netherlands.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2019 Jan 15;1105:10-14. doi: 10.1016/j.jchromb.2018.12.004. Epub 2018 Dec 6.

Abstract

Metabolomics studies using a small amount of cells may save time and money, while in some cases (e.g., profiling pathogenic cells in an early-stage tissue), only a small number of cells are accessible for analysis. The analysis of small amounts of biological samples challenges the analytical toolbox used in present-day metabolomics studies, and a significant number of crucial biological questions cannot be properly addressed. To allow metabolic profiling of limited sample amounts, the potential of capillary electrophoresis-mass spectrometry (CE-MS) using a sheathless porous tip interface has been assessed using HepG2 cells in starting amounts of 500 and 10,000 cells as a model system in this work. It is shown that highly efficient and information-rich metabolic profiles for cationic metabolites at low-pH separation conditions could be obtained by sheathless CE-MS using an injection volume of only circa 42 nL, which equals the content/aliquot of circa 0.25 and 5 HepG2 cells, respectively. With as little as the content of 0.25 cell injected, more than 24 cationic metabolites could be identified. A further improvement of sample preparation and/or the injection part is required in order to effectively analyze the compounds of interest in very low sample amounts by sheathless CE-MS. However, the results obtained so far clearly indicate the strong potential of the proposed method for metabolic profiling of limited sample amounts.

摘要

采用少量细胞的代谢组学研究可以节省时间和金钱,而在某些情况下(例如,在早期组织中分析致病细胞),仅可获得少量细胞进行分析。少量生物样本的分析对当前代谢组学研究中使用的分析工具提出了挑战,并且许多重要的生物学问题无法得到妥善解决。为了允许对有限的样本量进行代谢分析,本研究使用 HepG2 细胞作为模型系统,评估了使用无鞘多孔尖端接口的毛细管电泳-质谱(CE-MS)在起始量为 500 和 10,000 个细胞时的潜力。结果表明,通过仅使用约 42nL 的进样体积,在低 pH 分离条件下,可以对阳离子代谢物进行高效且信息丰富的代谢分析,该进样体积相当于每个细胞的内容物/等分物的约 0.25 和 5 个 HepG2 细胞。仅注射 0.25 个细胞的内容物,就可以鉴定出超过 24 种阳离子代谢物。需要进一步改进样品制备和/或进样部分,以便通过无鞘 CE-MS 有效地分析非常少量样本中的目标化合物。但是,迄今为止获得的结果清楚地表明,该方法对于有限样本量的代谢分析具有很大的潜力。

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