条形码
解码方法
计算机科学
DNA
单色
荧光
核酸
生物系统
编码(内存)
多路复用
计算生物学
寡核苷酸
纳米技术
化学
发光
杂交探针
分子探针
核酸热力学
解耦(概率)
生物物理学
信号(编程语言)
材料科学
光谱成像
DNA–DNA杂交
微流控
荧光显微镜
作者
Dandan Tian,Jianqing Yang,Linghao Zhang,Huixiao Yang,Shihui Wang,Xin Su
标识
DOI:10.1038/s41467-025-67410-3
摘要
Multiplexed nucleic-acid detection is essential for molecular diagnostics and spatial genomics, but conventional fluorescence methods are often limited by spectral overlap, nonspecific signals, and restricted encoding capacity. We present a spatial fluorescence barcode (SFB) platform based on transiently luminescent DNA beads (TLDBs) that enables single-color, high-plex readout. In this method, targets are encoded through the spatial arrangement of DNA-functionalized beads, eliminating the need for multicolor labeling or spectral unmixing. Target recognition is achieved through toehold-mediated strand displacement, and built-in nucleases enable autonomous enzymatic resetting for repeated use of probes. The system employs monochromatic spatial encoding, decoupling encoding capacity from spectral channels, and features a simplified probe design and decoding workflow. Self-resetting probes not only streamline the encoding process but also enhance practicality by allowing repeated assays without the need to re-prepare costly probe combinations. We demonstrate robust detection of pathogen-derived nucleic acids in infected blood and cancer-associated microRNAs in tissue samples, validating the platform's clinical applicability. Compared to existing barcoding strategies, SFB integrates monochromatic spatial encoding, simplified design, and autonomous reusability, offering a practical, scalable, and cost-effective solution for high-throughput nucleic acid analysis.
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