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Assembly of ordered microsphere arrays: Platforms for microarrays.

机译:组装有序微球阵列:微阵列平台。

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摘要

Microarrays are powerful tools in gene expression assessment, protein profiling, and protein function screening, as well as cell and tissue analysis. With thousands of small array spots assembled in an ordered array, these small devices makes it possible to screen for multiple targets in a fast, parallel, high-throughput manner. The well-developed technology of DNA microarrays, also called DNA chips, has proved successful in all kinds of biological experiments, including the human genome-sequencing project. The development of protein arrays has lagged behind that of DNA arrays mainly because of the greater complexity of proteins. Some parts of the microarray technology can be transplanted into the realm of protein arrays, while others cannot. The challenges from the complexity of protein targets demand more robust and powerful devices.;Traditional planar arrays, in which proteins bind directly to a planar surface, have a drawback in that some proteins will be denatured or cluster together after immobilization. Microsphere-based microarrays represent a more advanced strategy. The functional proteins are first attached to microspheres; these microspheres are then immobilized in arrays on a planar surface.;In this dissertation, two approaches to assembling arrays of microspheres will be discussed. The hydrodynamic approach uses surface micromachining and Deep Reactive Ion Etching techniques to form an array of channels through a silicon wafer. By drawing fluid containing the microspheres through the channels they become trapped in the channels and thereby immobilized. In the magnetic approach, permalloy films are deposited on a silicon substrate and subsequently patterned to form magnetic attachment sites. An external magnetic field is then applied and the magnetic microspheres then assemble on these sites. Both devices are able to immobilize microspheres in an ordered array, as opposed to coarsely grouping them in array spots. The assembled arrays are robust in that they ensure a resolution rate of almost 100%. In addition, different patterns of array spots with various spacings and diameters can be fabricated to satisfy different requirements. Moreover, the devices are easy to clean and reuse, and the experimental set-ups are relatively simple and portable. All these features make them good platforms for all kinds of microarrays.
机译:微阵列是基因表达评估,蛋白质谱分析,蛋白质功能筛选以及细胞和组织分析中的强大工具。通过将成千上万个小的阵列点组装成有序阵列,这些小型设备可以快速,并行,高通量的方式筛选多个目标。先进的DNA微阵列技术(也称为DNA芯片)已在包括人类基因组测序项目在内的各种生物实验中获得成功。蛋白质阵列的发展落后于DNA阵列,主要是因为蛋白质的复杂性更高。微阵列技术的某些部分可以移植到蛋白质阵列领域,而其他部分则不能。蛋白质靶标复杂性带来的挑战需要更坚固,功能强大的设备。传统的平面阵列(蛋白质直接结合到平面表面)具有一个缺点,即某些蛋白质在固定后会变性或聚集在一起。基于微球的微阵列代表了更高级的策略。功能蛋白首先附着在微球上;然后将这些微球固定在一个平面上的阵列中。本文将讨论两种组装微球阵列的方法。流体动力学方法使用表面微加工和深度反应离子刻蚀技术形成穿过硅晶片的通道阵列。通过将包含微球的流体通过通道吸走,它们就被困在通道中并因此被固定。在磁性方法中,坡莫合金膜沉积在硅基板上,随后被图案化以形成磁性附着位点。然后施加外部磁场,然后将磁性微球聚集在这些位置上。这两种设备都能够将微球固定在有序阵列中,而不是将它们粗略地排列在阵列点中。组装后的阵列坚固耐用,可确保几乎100%的分辨率。另外,可以制造具有各种间距和直径的阵列点的不同图案以满足不同的要求。此外,该设备易于清洁和重复使用,并且实验装置相对简单且便于携带。所有这些功能使它们成为各种微阵列的良好平台。

著录项

  • 作者

    Xu, Wanling.;

  • 作者单位

    Northwestern University.;

  • 授予单位 Northwestern University.;
  • 学科 Physics General.;Biophysics General.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 92 p.
  • 总页数 92
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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