Lin Weiming, Ding Tao, He Die, Zhang Nan, Li Haodong, Luo Wenjian, Wei Zhongxia, Ke Min, Jia Sisi, Fan Chunhai, Liang Le
The Institute for Advanced Studies (IAS), Department of Ophthalmology, Zhongnan Hospital of Wuhan University, State Key Laboratory of Metabolism and Regulation in Complex Organisms, College of Life Sciences, Wuhan University, Wuhan 430072, China.
Zhangjiang Laboratory, Shanghai 201210, China.
JACS Au. 2025 May 12;5(5):2123-2134. doi: 10.1021/jacsau.5c00058. eCollection 2025 May 26.
Nanodiamonds (NDs) with nitrogen-vacancy (NV) centers are emerging as powerful quantum nanosensors (QNs) in biomedical applications due to their exceptional sensitivity. However, achieving optimal diagnostics performance necessitates both high sensitivity and selectivity; especially in practical biomedical settings, it remains challenging for QNs to provide quantitative analyses when multiple analytes are present. Here, we present a biosensing platform that integrates DNA logic gates (DLGs) with spin-based quantum sensing, termed DLG-QN for ultrasensitive and ultraselective diagnostics. Utilizing an AND DLG, both NDs and magnetic beads (MBs) are functionalized with hairpin DNA strands. In the presence of both miRNA-21 and miRNA-155key biomarkers overexpressed in cancerthe hairpin DNAs undergo conformational changes that facilitate DNA-guided self-assembly of NDs and MBs, enriching the target signal. Resonant microwave modulation of ND fluorescence emission allows for high signal-to-noise ratio (SNR) detection by separating the signal from background fluorescence via spin-enhanced analysis. This platform demonstrated ultrasensitive and ultraselective detection of miRNA-21 and miRNA-155 with a limit of detection of 19.8 fM, highlighting its potential as a general biosensing strategy for precision diagnostics involving multiple biomarkers.
具有氮空位(NV)中心的纳米金刚石(NDs)因其卓越的灵敏度,正在成为生物医学应用中强大的量子纳米传感器(QNs)。然而,要实现最佳诊断性能,既需要高灵敏度又需要高选择性;特别是在实际生物医学环境中,当存在多种分析物时,QNs进行定量分析仍然具有挑战性。在此,我们提出了一种生物传感平台,该平台将DNA逻辑门(DLGs)与基于自旋的量子传感相结合,称为DLG-QN,用于超灵敏和超选择性诊断。利用与门DLG,NDs和磁珠(MBs)都用发夹DNA链进行功能化。在miRNA-21和miRNA-155(癌症中过表达的关键生物标志物)同时存在的情况下,发夹DNA会发生构象变化,从而促进NDs和MBs的DNA引导自组装,增强目标信号。通过自旋增强分析将信号与背景荧光分离,对ND荧光发射进行共振微波调制可实现高信噪比(SNR)检测。该平台展示了对miRNA-21和miRNA-155的超灵敏和超选择性检测,检测限为19.8 fM,突出了其作为涉及多种生物标志物的精确诊断通用生物传感策略的潜力。