Entropy-Driven Disassembly of Logic-Gated DNA Nanospheres: An All-in-One Platform for Precise Cancer Diagnosis In Vivo

DNA 计算生物学 癌症 计算机科学 生物 纳米技术 逻辑门 癌细胞 信号(编程语言) 小RNA DNA损伤 体内 癌症研究 癌症生物标志物 灵敏度(控制系统) 生物系统 多路复用 和大门 核酸 化学 杂交探针 A-DNA 癌症检测 材料科学 寡核苷酸 细胞生物学
作者
Jiaoli Wang,Shiyuan Liu,Xiaoyi Liu,Yu Chen,Jianbo Liu,Kemin Wang,Ke Quan,Jin Huang
出处
期刊:ACS Nano [American Chemical Society]
卷期号:19 (45): 39420-39429 被引量:11
标识
DOI:10.1021/acsnano.5c15156
摘要

DNA logic circuits, which can accurately identify specific cancer cell types, hold promise for the construction of emerging diagnostic platforms. However, they are challenged by weak output signals owing to the low abundance of biomarkers as well as the lack of an integrated, self-contained system for efficient circuit delivery that operates without extrinsic carriers. Herein, we developed all-in-one DNA nanospheres for precise cancer diagnosis that incorporate target recognition, logic analysis, signal amplification, and signal output within a single logic-gated DNA nanosphere, requiring no exogenous carriers or proteases. Programmable self-assembly of Y-shaped and I-shaped DNA motifs through sequence-specific hybridization enables the precise spatial organization of functional elements into nanosphere-shaped delivery vectors. Employing oncogenic miR-21 and/or miR-155 as molecular inputs, the DNA nanosphere performs AND or OR Boolean logic operations, which trigger entropy-driven disassembly that generates amplified fluorescence signals for multiplexed miRNA imaging. The platform exhibits a significantly enhanced biostability and sensitivity for identifying specific cancer cells. Through intratumoral injection, it achieves efficient in vivo delivery, enabling precise distinction between specific cancer cells and tumor types. The multi-miRNA-responsive molecular Boolean logic, in combination with entropy-driven disassembly, facilitates autonomous diagnostics operations, thus offering alternative design paradigms for accurate molecular diagnostics by using DNA logic systems.
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