DNA
连锁反应
化学
核糖核酸
DNA纳米技术
生物物理学
生物传感器
荧光
DNA–DNA杂交
环介导等温扩增
A-DNA
纳米结构
核酸热力学
渡线
杂交探针
动力学
材料科学
纳米技术
组合化学
DNA测序
复式(建筑)
核酸
分子生物物理学
分子信标
分支迁移
化学动力学
费斯特共振能量转移
作者
Pengda Liang,Xiao Wang
出处
期刊:Small
[Wiley]
日期:2025-12-19
卷期号:22 (9): e10431-e10431
被引量:1
标识
DOI:10.1002/smll.202510431
摘要
The classic hybridization chain reaction (HCR) is applied to paranemic crossover (PX) DNA structures, which generates assembled DNA nanostructures instead of linear DNA duplexes. As an analog of the stem-loop structure, PX structures with terminal loops and toeholds are designed as HCR reaction monomers. Isothermal strand displacement reaction on the PX-loop structure is studied, and the following PX-based HCR is carried out with both single-stranded DNA and RNA as the initiator. Furthermore, 2'-OMe modifications of the toehold and PX are used to enhance the binding to RNA, which optimized the kinetics of RNA initiated PX-HCR. In addition, paranemic crossover structures with the minimal paranemic cohesion are designed for microRNA triggered PX-HCR based on the 2'-OMe strategy, with a visible fluorescence response in minutes, suggesting the generality of this strategy. The facile initiation of HCR reaction on PX with both DNA and RNA indicates its potential for biosensing applications as well as assembling complex DNA nanostructures in the future.
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