化学
小RNA
检出限
DNA
纳米技术
癌细胞
计算生物学
癌症
计算机科学
生物化学
基因
遗传学
材料科学
色谱法
生物
作者
Saimei Zhang,Jiang Xue Dong,Yanping Zhao,Congcong Wang,Yajie Fan,Yanlei Li,Ming Su,Na Li,Shigang Shen,Zhong Feng Gao,Fan Xia
标识
DOI:10.1021/acs.analchem.5c02598
摘要
Finely tunable detection of microRNAs (miRNAs) is crucial for personalized medicine and cancer diagnosis, and it is a challenge to construct a tunable sensor for miRNA detection due to the diversity and complexity of cancer patient samples. This study introduces a three-dimensional (3D) DNA walker mediated by a remote toehold strand displacement reaction, which addresses the challenge of achieving tunable detection limits and sensitivities for microRNA-21 (miR-21) at a kinetic level, enabling specific recognition of cancer cells. By engineering a spacer domain within the DNA walker, the kinetics of the strand displacement reaction can be precisely modulated, thereby controlling the walking efficiency and achieving tunable detection with a detection limit range from 32 aM to 290 pM and a broad dynamic range from ∼1100-fold to ∼283,000-fold. This approach leverages the programmability of DNA molecules to design probe structures tailored to experimental requirements, offering high sensitivity and specificity and a wide detection limit. The 3D DNA walker, driven by Zn 2+, allows for rapid and accurate imaging of miR-21 in cancer cells, thereby effectively differentiating cancerous cells from normal cells. The proposed method not only demonstrates a high degree of specificity in recognizing miR-21 but also provides a robust foundation for clinical diagnosis and holds promise for applications in personalized medicine, early disease detection, and drug development. These findings underscore the potential of this remote toehold-mediated DNA walker as a powerful tool for real-time monitoring and dynamic detection of disease biomarkers, enhancing the precision and efficacy of therapeutic interventions.
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