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High throughput sample preparation and analysis for DNA sequencing, PCR and combinatorial screening of catalysis based on capillary array technique.

机译:基于毛细管阵列技术的高通量样品制备和分析,用于DNA测序,PCR和组合催化筛选。

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摘要

The purpose of this research was to develop new sample preparation and integration approach for DNA sequencing, PCR based DNA analysis and combinatorial screening of homogenous catalysis based on multiplexed capillary electrophoresis.;We first introduced a method to integrate the front-end tasks to DNA capillary-array sequencers. Protocols for directly sequencing the plasmids from a single bacterial colony in fused-silica capillaries were developed. No deleterious effect upon the reaction efficiency, the on-line purification system, or the capillary electrophoresis separation was observed, even though the crude lysate was used as the template. Multiplexed on-line DNA sequencing data from 8 parallel channels allowed base calling up to 620 bp with an accuracy of 98%. The entire system can be automatically regenerated for repeated operation.;For PCR based DNA analysis, we demonstrated that UV absorption capillary electrophoresis can be used for DNA analysis starting from clinical sample without purification. After PCR reaction using cheek cell, blood or HIV-1 gag DNA, the reaction mixture was injected into the capillary either on-line or off-line by base stacking. The protocol was also applied to capillary array electrophoresis based simply on multiplexed UV imaging absorption detection to increase the throughput.;We further developed a new methodology-nonaqueous capillary array electrophoresis coupled with microreaction, to address the throughput needs of combinatorial approaches to homogeneous catalysis screening and reaction optimization. Samples were injected directly from reaction vial without dilution and reaction quenching. Buffer compatibility was also found important for reliable 96-capillary array injection. By choosing deferent Pd and base, a combination of 88 different reaction conditions was quickly tested. The analysis time was less than one minute for one sample.
机译:这项研究的目的是为基于多重毛细管电泳的DNA测序,基于PCR的DNA分析和均相催化的组合筛选开发新的样品制备和整合方法。我们首先介绍了一种将前端任务整合到DNA毛细管中的方法-阵列定序器。已经开发出了直接对来自熔融石英毛细管中单个细菌菌落的质粒进行测序的方案。即使将粗裂解物用作模板,也未观察到对反应效率,在线纯化系统或毛细管电泳分离的有害影响。来自8个并行通道的多路在线DNA测序数据允许碱基检出速率高达620 bp,准确度达98%。整个系统可自动再生以重复操作。对于基于PCR的DNA分析,我们证明了紫外线吸收毛细管电泳可用于从临床样品开始的DNA分析,而无需纯化。使用脸颊细胞,血液或HIV-1 gag DNA进行PCR反应后,通过碱基堆叠将反应混合物在线或离线注入毛细管中。该协议还简单地应用于基于多重UV成像吸收检测的毛细管阵列电泳,以提高通量。;我们进一步开发了一种新方法-非水毛细管阵列电泳与微反应相结合,以满足组合方法进行均相催化筛选的通量需求和反应优化。直接从反应瓶中进样,无需稀释和反应淬灭。还发现缓冲液相容性对于可靠的96毛细管阵列进样非常重要。通过选择不同的Pd和碱,可以快速测试88种不同反应条件的组合。一个样品的分析时间少于一分钟。

著录项

  • 作者

    Zhang, Yonghua.;

  • 作者单位

    Iowa State University.;

  • 授予单位 Iowa State University.;
  • 学科 Analytical chemistry.
  • 学位 Ph.D.
  • 年度 2000
  • 页码 98 p.
  • 总页数 98
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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