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Distinguishing Single- and Double-Stranded Nucleic Acid Molecules Using Solid-State Nanopores

机译:使用固态纳米孔区分单链和双链核酸分子

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Solid-state nanopores offer a promising method for rapidly probing the structural properties of biopolymers such as DNA and RNA, We have for the first time translocated RNA molecules through solid-state nanopores, comparing the signatures of translocating double-stranded RNA molecules and of single-stranded homopolymers poly(A), poly(U), poly(C). On the basis of their differential blockade currents, we can rapidly discriminate between both single- and double-stranded nucleic-acid molecules, as well as separate purine-based homopolymers from pyrimidine-based homopolymers. Molecule identification is facilitated through the application of high voltages (similar to 600 mV), which contribute to the entropic stretching of these highly flexible molecules. This striking sensitivity to relatively small differences in the underlying polymer structure greatly improves the prospects for using nanopore-based devices for DNA or RNA mapping.
机译:固态纳米孔为快速探测生物聚合物(如DNA和RNA)的结构特性提供了一种有前途的方法。我们首次通过固态纳米孔对RNA分子进行了移位,比较了双链RNA分子和单链RNA分子易位的特征。链均聚物poly(A),poly(U),poly(C)。基于它们的不同阻断电流,我们可以快速区分单链和双链核酸分子,以及从嘧啶基均聚物中分离出嘌呤基均聚物。施加高压(类似于600 mV)有助于分子鉴定,这有助于这些高度柔性分子的熵拉伸。对基础聚合物结构中相对较小差异的显着敏感性极大地改善了使用基于纳米孔的设备进行DNA或RNA定位的前景。

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