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用 DNA 载体和固态纳米孔监测 G-四链体形成。

Monitoring G-Quadruplex Formation with DNA Carriers and Solid-State Nanopores.

机构信息

Cavendish Laboratory , University of Cambridge , JJ Thompson Avenue , Cambridge CB3 0HE , United Kingdom.

出版信息

Nano Lett. 2019 Nov 13;19(11):7996-8001. doi: 10.1021/acs.nanolett.9b03184. Epub 2019 Oct 10.

Abstract

G-quadruplexes (Gqs) are guanine-rich DNA structures formed by single-stranded DNA. They are of paramount significance to gene expression regulation, but also drug targets for cancer and human viruses. Current ensemble and single-molecule methods require fluorescent labels, which can affect Gq folding kinetics. Here we introduce, a single-molecule Gq nanopore assay (smGNA) to detect Gqs and kinetics of Gq formation. We use ∼5 nm solid-state nanopores to detect various Gq structural variants attached to designed DNA carriers. Gqs can be identified by localizing their positions along designed DNA carriers, establishing smGNA as a tool for Gq mapping. In addition, smGNA allows for discrimination of (un)folded Gq structures, provides insights into single-molecule kinetics of Gq folding, and probes quadruplex-to-duplex structural transitions. smGNA can elucidate the formation of Gqs at the single-molecule level without labeling and has potential implications on the study of these structures both in single-stranded DNA and in genomic samples.

摘要

G-四链体(Gqs)是由单链 DNA 形成的富含鸟嘌呤的 DNA 结构。它们对基因表达调控至关重要,但也是癌症和人类病毒的药物靶点。目前的整体和单分子方法需要荧光标记,这可能会影响 Gq 折叠动力学。在这里,我们引入了一种单分子 Gq 纳米孔检测方法(smGNA)来检测 Gqs 和 Gq 形成的动力学。我们使用约 5nm 的固态纳米孔来检测附着在设计 DNA 载体上的各种 Gq 结构变体。通过定位它们在设计的 DNA 载体上的位置,可以识别 Gqs,从而确立 smGNA 作为 Gq 作图的工具。此外,smGNA 允许区分(未)折叠的 Gq 结构,提供对 Gq 折叠的单分子动力学的深入了解,并探测四链体-双链体结构转变。smGNA 可以在不进行标记的情况下在单分子水平上阐明 Gqs 的形成,这对研究单链 DNA 和基因组样本中的这些结构具有潜在意义。

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