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Magneto-fluorescent nanobiosensor with tetrahedral framework nucleic acid-confined aptamer for trace adenosine triphosphate detection

适体 荧光 核酸 化学 生物传感器 生物物理学 纳米探针 三磷酸腺苷 分析物 组合化学 分子信标 DNA 纳米技术 色谱法 生物化学 寡核苷酸 材料科学 分子生物学 纳米颗粒 生物 量子力学 物理
作者
Guobin Huang,Qian Xie,Jinxin Chi,Chenchen Lin,Xucong Lin,Zenghong Xie
出处
期刊:Sensors and Actuators B-chemical [Elsevier]
卷期号:417: 136129-136129 被引量:2
标识
DOI:10.1016/j.snb.2024.136129
摘要

Accurate quantitation of trace-level ATP biomarkers often suffers from interference of sample matrix and remains a challenge. Herein, a novel magnetic biological nanosensor (MBNS) integrating tetrahedral framework nucleic acid (tFNA)-confined aptamers and ultrasensitive laser-induced fluorescence (LIF) was tailored and evaluated. The fluorescent aptamer nanoprobe hybridized with FAM-labelled cDNA was particularly incorporated into the inner cavity of tFNA, enabling a dual-mode mechanism that integrates molecular size selection and aptamer affinity recognition. By this strategy, the benefits of tFNA molecular sieve, the super sensitive properties of LIF, and the specific recognition of "aptamer gene codes" were integrated, as triggered the superior response of ATP. The structures, properties and reaction mechanism of tFNA, as well as tFNA modified with aptamer probe at different sites, were characterized in detail. A high level of anti-interference was achieved, shielding against non-specific adsorption even in matrices with high protein and analogue content, 103∼105 times higher than ATP. The release of fluorescent beacon from aptamer probe was facilely driven by specific binding of ATP, and an ultra-sensitive detection of 75 pmol/L ATP was obtained without amplification. It was 2–3 orders of magnitude more sensitive than most fluorescent aptasensors. Applied to serum samples, the stability and reproducibility of the resultant aptasensor have been validated with the intra- and inter-assay RSD in 1.6–6.4 % and -1.5–8.4 %, respectively. Acceptable recoveries of 96.5–106.8 % were achieved, consistent with the LC-MS method. It was expected to open a simple and efficient protocol for highly specific and ultrasensitive ATP detection in clinical diagnostics.
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