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首页> 外文期刊>Analytical chemistry >Consecutive Gated Injection-Based Microchip Electrophoresis for Simultaneous Quantitation of Superoxide Anion and Nitric Oxide in Single PC-12 Cells
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Consecutive Gated Injection-Based Microchip Electrophoresis for Simultaneous Quantitation of Superoxide Anion and Nitric Oxide in Single PC-12 Cells

机译:连续门控基于注射的微芯片电泳同时定量单个PC-12细胞中的超氧阴离子和一氧化氮

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As important reactive oxygen species (ROS) and reactive nitrogen species (ENS), cellular superoxide anion (O-2(center dot-)) and nitric oxide (NO) play significant roles in numerous physiological and pathological processes. Cellular O-2(center dot-) NO also have a close relationship and always interact with each other. Thus, the simultaneous detection of intracellular O-2(center dot-) and NO, especially at the single-cell level, is important. In this paper, we present a novel method to simultaneously detect and quantify O-2(center dot-) and NO in single cells using microchip electrophoresis based on a new consecutive gated injection method. This novel injection method achieved consecutive manipulation of single cells, guaranteeing an almost constant volumetric flow rate and thus good quantitative reproducibility. After cellular content separation by microchip electrophoresis and detection by laser-induced fluorescence (MCE-LIF), O-2(center dot-) and NO in single PC-12 cells were simultaneously quantified in an automated fashion. This is the first report of consecutive absolute quantitation at the single-cell level. The quantitative results obtained from single cells is beneficial for deep understanding of the biological roles of cellular O-2(center dot-) and NO. This new method constitutes a consecutive, accurate way to study the synergistic function of O-2(center dot-) and NO and other biomolecules in various biological events at the single-cell level.
机译:作为重要的活性氧(ROS)和活性氮(ENS),细胞超氧阴离子(O-2(中心点))和一氧化氮(NO)在许多生理和病理过程中起着重要作用。细胞的O-2(中心点)NO也有密切的关系,并且总是相互影响。因此,同时检测细胞内O-2(中心点)和NO尤其重要,尤其是在单细胞水平上。在本文中,我们提出了一种新的方法,该方法基于一种新的连续门控注入方法,利用微芯片电泳同时检测和定量单个细胞中的O-2(中心点)和NO。这种新颖的进样方法实现了对单个细胞的连续操作,从而保证了几乎恒定的体积流速,因此具有良好的定量重现性。通过微芯片电泳分离细胞含量并通过激光诱导荧光(MCE-LIF)检测后,以自动化方式同时定量单个PC-12细胞中的O-2(中心点)和NO。这是单细胞水平上连续绝对定量分析的首次报道。从单个细胞获得的定量结果有助于深入了解细胞O-2(中心点)和NO的生物学作用。这种新方法构成了一种连续,准确的方法,用于在单细胞水平上研究O-2(中心点)与NO和其他生物分子在各种生物事件中的协同作用。

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