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Automated Optically Guided System for Chemical Analysis of Single Plant and Algae Cells Using Laser Microdissection/Liquid Vortex Capture/Mass Spectrometry

机译:自动化光学导引系统用于使用激光显微切割/液体涡旋捕获/质谱法对单个植物和藻类细胞进行化学分析

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摘要

Current analytical methods are not capable of providing rapid, sensitive, and comprehensive chemical analysis of a wide range of cellular constitutes of single cells (e.g., lipids, metabolites, proteins, etc.) from dispersed cell suspensions and thin tissues. This capability is important for a number of critical applications, including discovery of cellular mechanisms for coping with chemical or environmental stress and cellular response to drug treatment, to name a few. Here we introduce an optically guided platform and methodology for rapid, automated recognition, sampling, and chemical analysis of surface confined individual cells utilizing a novel hybrid laser capture microdissection/liquid vortex capture/mass spectrometry system. The system enabled automated analysis of single cells by reliably detecting and sampling them either through laser ablation from a glass microscope slide or by cutting the entire cell out of a poly(ethylene naphthalate)-coated membrane substrate that the cellular sample is deposited on. Proof of principle experiments were performed using thin tissues of Allium cepa and cultured Euglena gracilis and Phacus cell suspensions as model systems for single cell analysis using the developed method. Reliable, hands-off laser ablation sampling coupled to liquid vortex capture/mass spectrometry analysis was conducted for hundreds of individual Allium cepa cells in connected tissue. In addition, more than 300 individual Euglena gracilis and Phacus cells were analyzed automatically and sampled using laser microdissection sampling with the same liquid vortex capture/mass spectrometry analysis system. Principal component analysis-linear discriminant analysis, applied to each mass spectral dataset, was used to determine the accuracy of differentiation of the different algae cell lines.
机译:当前的分析方法不能对分散的细胞悬液和薄组织中的单个细胞的多种细胞组成(例如脂质,代谢产物,蛋白质等)进行快速,灵敏和全面的化学分析。此功能对许多关键应用很重要,包括发现用于应对化学或环境胁迫的细胞机制以及细胞对药物治疗的反应等。在这里,我们介绍一种光学引导平台和方法,利用新型的混合激光捕获显微切割/液体涡流捕获/质谱系统对表面受限的单个细胞进行快速,自动识别,采样和化学分析。该系统通过可靠地从玻璃显微镜载玻片上进行激光消融或通过从沉积有细胞样品的聚萘二甲酸乙二醇酯薄膜基质中切出整个细胞来可靠地检测和采样单个细胞,从而实现了对单个细胞的自动分析。使用洋葱的稀薄组织和培养的裸藻和Phacus细胞悬液作为模型系统,使用开发的方法进行原理验证实验。对连接的组织中的数百个单独的洋葱cepa细胞进行了可靠的,无需人工干预的激光消融采样,并结合了液体涡流捕获/质谱分析。此外,使用相同的液体涡流捕获/质谱分析系统,自动分析了300多个单个的Euglena gracilis和Phacus细胞,并使用激光显微解剖采样对其进行了采样。将主成分分析-线性判别分析应用于每个质谱数据集,以确定不同藻类细胞系分化的准确性。

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