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通过 ZIF-8 的原位生物矿化即时生成纳米标签,实现未经修饰电极上的超灵敏 microRNA 检测。

Just-in-Time Generation of Nanolabels via In Situ Biomineralization of ZIF-8 Enabling Ultrasensitive MicroRNA Detection on Unmodified Electrodes.

机构信息

Fujian Key Laboratory for Translational Research in Cancer and Neurodegenerative Diseases, School of Basic Medical Sciences, Fujian Medical University, Fuzhou 350122, China.

Department of Cardio thoracic Surgery, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, Fujian 350025, China.

出版信息

Anal Chem. 2024 Oct 22;96(42):16793-16801. doi: 10.1021/acs.analchem.4c03434. Epub 2024 Oct 11.

DOI:10.1021/acs.analchem.4c03434
PMID:39391952
Abstract

Nanolabels can enhance the detection performance of electrochemical biosensing methods, yet their practical application is hindered by complex preparation, batch-to-batch variability, and poor long-term storage stability. Herein, we present a novel electrochemical method for miRNA detection based on the just-in-time generation of zeolitic imidazolate framework-8 (ZIF-8) nanolabels initiated by nucleic acids. In this design, the target miRNA-21 is captured with magnetic beads and polyadenylated by Poly(A) polymerase (PP), producing miRNA-21 molecules with poly(A) tails (miR-21-poly(A)). These molecules are then adsorbed onto a bare gold electrode (AuE) surface via adenine-gold affinity interactions, serving as nucleation sites for the rapid formation of ZIF-8 nanoparticles. The ZIF-8 nanoparticles function as signal labels, impeding electron transfer at the electrode interfaces and thereby generating a notable electrochemical signal. The developed method demonstrated exceptional sensitivity, with a detection limit (LOD) as low as 2.3 aM and a linear detection range from 10 aM to 1000 fM. The practical application of the developed method was validated by using it to evaluate miRNA-21 expression levels in various biological samples, including cell lines, tumor tissues, and clinical blood samples from non-small cell lung cancer (NSCLC) patients. This approach simplifies the detection process by eliminating the need for presynthesized nanomaterials and premodified electrodes. Its simplicity and high sensitivity make this method a promising tool for point-of-care testing and a wide range of biomedical research applications.

摘要

纳米标签可以增强电化学生物传感方法的检测性能,但由于其复杂的制备、批间变异性和较差的长期储存稳定性,其实际应用受到限制。在此,我们提出了一种基于核酸引发的沸石咪唑酯骨架-8(ZIF-8)纳米标签即时生成的新型电化学 miRNA 检测方法。在该设计中,靶 miRNA-21 被磁珠捕获,并通过 Poly(A) 聚合酶(PP)多聚腺苷酸化,产生带有 Poly(A) 尾巴的 miRNA-21 分子(miR-21-poly(A))。这些分子通过腺嘌呤-金亲和力相互作用吸附到裸金电极(AuE)表面上,作为 ZIF-8 纳米颗粒快速形成的成核位点。ZIF-8 纳米颗粒作为信号标签,阻碍电极界面处的电子转移,从而产生显著的电化学信号。所开发的方法表现出出色的灵敏度,检测限(LOD)低至 2.3 aM,线性检测范围从 10 aM 到 1000 fM。通过使用该方法评估来自非小细胞肺癌(NSCLC)患者的各种生物样本中的 miRNA-21 表达水平,验证了所开发方法的实际应用,包括细胞系、肿瘤组织和临床血样。该方法通过消除对预合成纳米材料和预修饰电极的需求,简化了检测过程。其简单性和高灵敏度使该方法成为即时检测和广泛的生物医学研究应用的有前途的工具。

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