DNA
核酸
计算生物学
脱氧核酶
序列(生物学)
蛋白质检测
肽核酸
碱基对
化学
互补序列
DNA测序
计算机科学
肽
寡核苷酸
变性(裂变材料)
基序列
人类蛋白质
复式(建筑)
生物
核酸热力学
肽序列
基础(拓扑)
核酸序列
A-DNA
生物物理学
分子生物学
分子生物物理学
生物系统
作者
Jiaqi Yan,Rajendra Bhadane,Wentao Xu,Meixin Ran,Xiaochao Ma,Yuanqiang Li,Kevin Jahnke,Xiaodong Ma,Outi M. H. Salo-Ahen,Mauri A. Kostiainen,David A. Weitz,Hongbo Zhang
标识
DOI:10.1073/pnas.2515765123
摘要
Current methodologies for detecting the sequence of double-stranded DNA (dsDNA) require amplifying and denaturing the target into single-stranded DNA (ssDNA) to enable sequence detection through Watson-Crick base pairing. However, these approaches are limited by the risks of nonspecific amplification, reliance on complex, temperature-sensitive protein enzymes, and harsh reaction conditions, such as in strong base or acidic environments. Here, we introduce a dsDNA detection platform that integrates a peptide nucleic acid (PNA) as the dsDNA denaturation agent, with multicomponent deoxyribozyme as the ssDNA detection tool, in a droplet-based system. This protein- and amplification-free method offers single-nucleotide resolution, detects down to a single dsDNA molecule, and delivers results within 1 h at room temperature. This work introduces a conceptually unique approach, that may be useful for both diagnostics and therapeutics.
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