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采用大体积进样堆积毛细管电泳技术在手性测定单个神经元中的天冬氨酸和谷氨酸。

Chiral Measurement of Aspartate and Glutamate in Single Neurons by Large-Volume Sample Stacking Capillary Electrophoresis.

机构信息

Department of Chemistry and Beckman Institute, University of Illinois at Urbana-Champaign , Urbana, Illinois 61801, United States.

出版信息

Anal Chem. 2017 Nov 21;89(22):12375-12382. doi: 10.1021/acs.analchem.7b03435. Epub 2017 Nov 8.

Abstract

d-Amino acids (d-AAs) are endogenous molecules found throughout the metazoan, the functions of which remain poorly understood. Measurements of low abundance and heterogeneously distributed d-AAs in complex biological samples, such as cells and multicellular structures of the central nervous system (CNS), require the implementation of sensitive and selective analytical approaches. In order to measure the d- and l-forms of aspartate and glutamate, we developed and applied a stacking chiral capillary electrophoresis (CE) with laser-induced fluorescence detection method. The achieved online analyte preconcentration led to a 480-fold enhancement of detection sensitivity relative to capillary zone electrophoresis, without impacting separation resolution or analysis time. Additionally, the effects of inorganic ions on sample preconcentration and CE separation were evaluated. The approach enabled the relative quantification of d-aspartate and d-glutamate in individual neurons mechanically isolated from the CNS of the sea slug Aplysia californica, a well characterized neurobiological model. Levels of these structurally similar d-AAs were significantly different in subpopulations of cells collected from the investigated neuronal clusters.

摘要

d-氨基酸(d-AAs)是真核生物中存在的内源性分子,但其功能仍知之甚少。在复杂的生物样本(如细胞和中枢神经系统的多细胞结构)中,需要实施灵敏和选择性的分析方法来测量低丰度和不均匀分布的 d-AAs。为了测量天冬氨酸和谷氨酸的 d-和 l-形式,我们开发并应用了一种与激光诱导荧光检测相结合的在线堆积手性毛细管电泳(CE)方法。与毛细管区带电泳相比,实现的在线分析物预浓缩使检测灵敏度提高了 480 倍,而不影响分离分辨率或分析时间。此外,还评估了无机离子对样品预浓缩和 CE 分离的影响。该方法使我们能够对从加利福尼亚海兔 Aplysia californica 的中枢神经系统中机械分离的单个神经元中 d-天冬氨酸和 d-谷氨酸进行相对定量,这是一种具有良好特征的神经生物学模型。在所研究的神经元簇中收集的细胞亚群中,这些结构相似的 d-AAs 的水平存在显著差异。

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