堆积
信号(编程语言)
复制
分析物
DNA
生物传感器
计算机科学
生物系统
细胞内
放大器
小RNA
电子线路
纳米技术
计算生物学
生物物理学
材料科学
化学
物理
生物
光电子学
细胞生物学
遗传学
核磁共振
基因
统计
物理化学
量子力学
程序设计语言
CMOS芯片
数学
作者
Jie Wei,Mengdi Yu,Kaiyue Tan,Jinhua Shang,Shizhen He,Chenxia Xie,Xiaoqing Liu,Fuan Wang
出处
期刊:Small
[Wiley]
日期:2023-01-30
卷期号:19 (17)
被引量:14
标识
DOI:10.1002/smll.202207961
摘要
Abstract Trace analyte detection in complex intracellular environment requires the development of simple yet robust self‐sufficient molecular circuits with high signal‐gain and anti‐interference features. Herein, a minimal non‐enzymatic self‐replicate DNA circuitry (SDC) system is proposed with high‐signal‐gain for highly efficient biosensing in living cells. It is facilely engineered through the self‐stacking of only one elementary cascade hybridization reaction (CHR), thus is encoding with more economic yet effective amplification pathways and reactants. Trigger ( T ) stimulates the activation of CHR for producing numerous T replica that reversely motivate new CHR reaction cycles, thus achieving the successive self‐replication of CHR system with an exponentially magnified readout signal. The intrinsic self‐replicate circuity design and the self‐accelerated reaction format of SDC system is experimentally demonstrated and theoretically simulated. With simple circuitry configuration and low reactant complexity, the SDC amplifier enables the high‐contrast and accurate visualization of microRNA (miRNA), ascribing to its robust molecular recognition and self‐sufficient signal amplification, thus offering a promising strategy for monitoring these clinically significant analytes.
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