化学
荧光
生物系统
信号(编程语言)
DNA
生物物理学
共焦
胶体金
细胞内
放射性检测
亚细胞定位
纳米技术
费斯特共振能量转移
荧光寿命成像显微镜
A-DNA
共焦显微镜
寡核苷酸
单细胞分析
生物传感器
细胞
计算生物学
纳米颗粒
小RNA
过程(计算)
核酸
检出限
作者
Wenting Wei,Han Lin,Kuniharu Ijiro,Hideyuki Mitomo
标识
DOI:10.1021/acs.analchem.5c04705
摘要
Accurate detection of low-abundance microRNA (miRNA) as tumor biomarkers in body fluids and cells is critical due to its strong association with tumor initiation, progression, invasion, and metastasis. DNA walkers enable signal amplification through cyclic enzymatic reactions, offering powerful strategies for the highly sensitive detection of low-abundance miRNAs. However, fluctuations in the cellular microenvironment─such as variations in ion concentration, enzyme activity, temperature, and pH across subcellular compartments─can disrupt amplification efficiency and compromise detection accuracy. To address this challenge, we developed a symmetric bipedal DNA walker design in which one "leg" generates a detection signal while the other "reference leg" synchronously amplifies a dynamic (environment-responsive) internal reference signal. Unlike traditional static internal reference strategies, this design introduces a real-time, synchronized internal reference during the DNA walking process to correct for system errors. When combined with ratiometric fluorescence-based error compensation, this approach effectively eliminates signal variation caused by nanoparticle loading, strand assembly, and environmental fluctuations, thereby improving the detection precision and reproducibility. The system, constructed on gold nanoparticles using an inverted hairpin scaffold, demonstrated robust and consistent performance under varied experimental conditions. Confocal ratiometric fluorescence imaging enabled the high-contrast quantification of intracellular miRNA-21 (miR-21) levels across different cell lines. Moreover, spatially resolved fluorescence signals revealed heterogeneous miR-21 distribution within individual cells, providing valuable insights into its subcellular localization and functional relevance. This strategy represents a reliable platform for accurate miRNA quantification even in complex biological environments.
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