Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, Chongqing Engineering Laboratory of Nanomaterials & Sensor Technologies, School of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, PR China.
Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, Chongqing Engineering Laboratory of Nanomaterials & Sensor Technologies, School of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, PR China.
Biosens Bioelectron. 2024 Nov 1;263:116621. doi: 10.1016/j.bios.2024.116621. Epub 2024 Jul 31.
Constructing label-free bivariate fluorescence biosensor would be intriguing and desired for the recognizable and accurate detection of two specific DNA segments, yet the design of functional DNA structures with low overlapped interference might be challenging. Herein in this work, a double-faced Janus DNA nanoarchitecture (JDNA) with bi-responsive recognition regions on opposite sides was assembled, which consisted of two substrate strands and two template strands for loading green-/red-emissive Ag nanoclusters (gAgNC and rAgNC) as bivariate signaling reporters. Of note, the hybridized double helix in the middle rationally oriented two flank faces and stabilized the rigid conformation of JDNA, while the template sequences of bicolor clusters were blocked to minimize non-specific background leakage. Upon inputting two targets, the discernible hairpins lost their hairpin structures due to forming two dsDNA complexes. They were executed to simultaneously invade JDNA for activating two individual target-recycled strand displacement (TRSD) events, guiding signal transduction and efficient amplification. Consequently, the clustering templates were unlocked via the tailored conformation switch of JDNA, in which gAgNC and rAgNC were in situ synthesized in two diagonal positions, thereby significantly emitting bi-responsive signal without cross interference. Benefited from the logic integration of double-faced JDNA and TRSD, a label-free, sensitive and specific bivariate fluorescence approach was developed, which would open a new avenue for the potential application in biosensing and bioanalysis.
构建无标记的双变量荧光生物传感器对于识别和准确检测两个特定的 DNA 片段是有趣且需要的,但设计具有低重叠干扰的功能 DNA 结构可能具有挑战性。在这项工作中,组装了一种具有两面性的 Janus DNA 纳米结构(JDNA),其相对侧具有双响应识别区域,由两条底物链和两条模板链组成,用于加载绿色/红色发射的 Ag 纳米团簇(gAgNC 和 rAgNC)作为双变量信号报告器。值得注意的是,杂交双链在中间合理地定向两个侧翼面,并稳定 JDNA 的刚性构象,而双色簇的模板序列被阻断以最小化非特异性背景泄漏。当输入两个靶子时,由于形成两个 dsDNA 复合物,可分辨的发夹结构失去了其发夹结构。它们被执行以同时入侵 JDNA,从而激活两个独立的靶标循环链置换(TRSD)事件,引导信号转导和有效放大。因此,通过 JDNA 的定制构象开关解锁聚类模板,gAgNC 和 rAgNC 分别在两个对角位置原位合成,从而在没有交叉干扰的情况下发出明显的双响应信号。得益于双面 JDNA 和 TRSD 的逻辑集成,开发了一种无标记、敏感和特异的双变量荧光方法,为生物传感和生物分析中的潜在应用开辟了新途径。