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Sequence-specific Nucleic Acid Detection from Binary Pore Conductance Measurement

机译:二进制孔电导测量中的序列特异性核酸检测

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摘要

We describe a platform for sequence-specific nucleic acid (NA) detection utilizing a micropipet tapered to a 2 μm diameter pore and 3 μm diameter polystyrene beads to which uncharged peptide nucleic acid (PNA) probe molecules have been conjugated. As the target NAs hybridize to the complementary PNA-beads, the beads acquire negative charge and become electrophoretically mobile. An applied electric field guides these NA-PNA-beads toward the pipet tip, which they obstruct, leading to an indefinite, electrically detectable, partial blockade of the pore. In the presence of noncomplementary NA,even to the level of single base mismatch, permanent pore blockade is not seen. We show application of this platform to detection of the anthrax lethal factor sequence.
机译:我们描述了一个平台,用于利用锥形到直径为2μm的孔和直径为3μm的聚苯乙烯珠的微移液管进行序列特异性核酸(NA)检测,其中不带电的肽核酸(PNA)探针分子已与之结合。当目标NA与互补的PNA磁珠杂交时,磁珠获得负电荷并电泳移动。施加的电场将这些NA-PNA珠子引向移液器吸头,它们被阻塞,导致孔的不确定,电可检测的局部阻塞。在存在非互补NA时,即使达到单碱基错配的水平,也看不到永久的孔阻塞。我们展示了该平台在炭疽致死因子序列检测中的应用。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2012年第38期|p.15880-15886|共7页
  • 作者单位

    Department of Bioengineering, University of California, Los Angeles, California, United States;

    Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, California, United States;

    Department of Bioengineering, University of California, Los Angeles, California, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 03:13:38

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