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Development of analytical methodology for neurochemical investigations.

机译:神经化学研究分析方法的发展。

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摘要

The development of sensitive and selective analytical tools has facilitated the investigation of complex neurological pathways and enhanced our understanding of neurodegenerative diseases. The development of sensitive analytical methodology for the determination of neurotransmitters and proteins related to neurodegenerative disease is described. The goal of the work performed in the first part of this dissertation was to develop analytical methodology for the analysis of catecholamine neurotransmitters (NTs) by microchip electrophoresis with electrochemical (EC) detection. Much of this work focused on the fabrication and characterization of the novel carbon-based electrode material, pyrolyzed photoresist. The fabrication of pyrolyzed photoresist film (PPF) electrodes was optimized for use in microchip electrophoresis and analytical performance was characterized using catecholamine NTs. In addition, an extensive comparison of the analytical performance of several commonly used electrode materials and electrode alignment schemes and the PPF electrode material was performed. Aspects such as sensitivity, limit of detection (LOD), resolution, reproducibility, and ease of fabrication were examined.In addition to the development of EC detection methods for catecholamine NTs, analytical methods for the determination of myc-tagged proteins were developed. The development of an electrophoretic immunoaffinity assay for the detection of a myc-tagged protein expressed in cell culture is described. While this is a general assay that can be applied to a variety of myc-tagged proteins, mutant huntingtin protein (mHtt) was used as a specific example. The development and optimization of capillary and microchip electrophoresis assays were performed for this purpose. In addition, the results obtained using these methods were directly compared to traditional analysis by Western blotting. The long term goal of this project is integrate both of these assays into a single lab-on-a-chip device capable of detecting NT release and mHtt protein in single cells.
机译:灵敏和选择性分析工具的发展促进了复杂神经系统途径的研究,并增进了我们对神经退行性疾病的了解。描述了用于确定与神经退行性疾病有关的神经递质和蛋白质的灵敏分析方法的发展。本论文第一部分的工作目的是开发一种通过电化学检测(EC)的微芯片电泳分析儿茶酚胺神经递质(NTs)的分析方法。这项工作大部分集中在新型碳基电极材料热解光致抗蚀剂的制造和表征上。热解光致抗蚀剂薄膜(PPF)电极的制备经过优化,可用于微芯片电泳,并使用儿茶酚胺NTs表征分析性能。另外,对几种常用电极材料,电极对准方案和PPF电极材料的分析性能进行了广泛的比较。研究了灵敏度,检测限(LOD),分辨率,可重复性和易于制造等方面。除了开发儿茶酚胺NT的EC检测方法外,还开发了测定myc标记蛋白的分析方法。描述了用于检测细胞培养物中表达的myc标记蛋白的电泳免疫亲和测定方法的开发。尽管这是可以应用于多种带有myc标签的蛋白的常规检测方法,但突变亨廷顿蛋白(mHtt)被用作一个特定的例子。为此,进行了毛细管电泳和微芯片电泳分析的开发和优化。此外,将使用这些方法获得的结果与通过蛋白质印迹法进行的传统分析直接进行比较。该项目的长期目标是将这两种检测方法整合到一个能够检测单个细胞中NT释放和mHtt蛋白的单芯片实验室设备中。

著录项

  • 作者

    Fischer, David J.;

  • 作者单位

    University of Kansas.;

  • 授予单位 University of Kansas.;
  • 学科 Chemistry Analytical.Chemistry Pharmaceutical.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 325 p.
  • 总页数 325
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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