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Ultraspecific and Highly Sensitive Nucleic Acid Detection by Integrating a DNA Catalytic Network with a Label-Free Microcavity

机译:通过将DNA催化网络与无标记微腔相集成来进行超特异性和高灵敏度的核酸检测

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摘要

Nucleic acid detection with label-free biosensors circumvents costly fluorophore functionalization steps associated with conventional assays by utilizing transducers of impressive ultimate detection limits. Despite this technological prowess, molecular recognition at a surface limits the biosensors' sensitivity, specificity, and reusability. It is therefore imperative to integrate novel molecular approaches with existing label-free transducers to overcome those limitations. Here, we demonstrate this concept by integrating a DNA strand displacement circuit with a micron-scale whispering gallery mode (WGM) microsphere biosensor. The integrated biosensor exhibits at least 25-fold improved nucleic acid sensitivity, and sets a new record for label-free microcavity biosensors by detecting 80 pM (32 fmol) of a 22nt oligomer; this improvement results from the catalytic behavior of the circuit. Furthermore, the integrated sensor exhibits extremely high specificity; single nucleotide variants yield 40- to 100-fold lower signal. Finally, the same physical sensor was demonstrated to alternatingly detect 2 different nucleic acid sequences through 5 cycles of detection, showcasing both its reusability and its versatility.
机译:利用无标记生物传感器进行核酸检测,通过利用具有极高最终检测极限的传感器,可以避免与常规测定相关的昂贵的荧光团功能化步骤。尽管具有这项技术实力,但表面的分子识别仍限制了生物传感器的灵敏度,特异性和可重复使用性。因此,有必要将新颖的分子方法与现有的无标记换能器整合在一起,以克服这些限制。在这里,我们通过将DNA链置换电路与微米级回音壁模式(WGM)微球生物传感器集成来证明这一概念。集成的生物传感器显示出至少25倍的改进的核酸敏感性,并通过检测80 pM(32 fmol)的22nt寡聚物,创造了无标记微腔生物传感器的新记录;这种改进来自电路的催化性能。此外,集成传感器具有极高的特异性。单核苷酸变体产生的信号降低40到100倍。最终,同一物理传感器被证明可以通过5个检测周期交替检测2个不同的核酸序列,从而展示了其可重复使用性和多功能性。

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