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升级和发光生物传感平台:熵驱动催化电路操纵新型 DNA 银纳米簇在氧化石墨烯表面的构象转变。

Upgraded and Light-Up Biosensing Platform: Entropy-Driven Catalysis Circuit Manipulates the Configuration Transformation of Novel DNA Silver Nanoclusters on the Graphene Oxide Surface.

机构信息

School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, P. R. China.

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio-Nanotechnology and Molecular Engineering of Hunan Province, Hunan University, Changsha 410082, P. R. China.

出版信息

Anal Chem. 2024 Jun 4;96(22):9209-9217. doi: 10.1021/acs.analchem.4c01338. Epub 2024 May 20.

Abstract

To tackle the predicament of the traditional turn-off mechanism, exploring an activated turn-on system remains an intriguing and crucial objective in biosensing fields. Herein, a dark DNA Ag nanocluster (NC) with hairpin-structured DNA containing a six-base cytosine loop (6C loop) as a template is atypically synthesized. Intriguingly, the dark DNA Ag NCs can be lit to display strong red-emission nanoclusters. Building upon these exciting findings, an unprecedented and upgraded turn-on biosensing system [entropy-driven catalysis circuit (EDCC)-Ag NCs/graphene oxide (GO)] has been created, which employs an EDCC to precisely manipulate the conformational transition of DNA Ag NCs on the GO surface from adsorption to desorption. Benefiting from the effective quenching of GO and signal amplification capability of the EDCC, the newly developed EDCC-Ag NCs/GO biosensing system displays a high signal-to-background (S/B) ratio (26-fold) and sensitivity (limit of detection as low as 0.4 pM). Meanwhile, it has good specificity, excellent stability, and reliability in both buffer and biological samples. To the best of our knowledge, it is the first example that adopts an EDCC to precisely modulate the configuration transformation of DNA Ag NCs on the GO surface to obtain a biosensor with low background, strong fluorescence, high contrast, and sensitivity. This exciting finding may provide a new route to fabricate a novel turn-on biosensor based on hairpin-templated DNA Ag NCs in the optical imaging and bioanalytical fields.

摘要

为了解决传统关闭机制的困境,探索激活型开启系统仍然是生物传感领域一个有趣且至关重要的目标。在此,我们以发夹结构 DNA 为模板,非典型地合成了具有六碱基胞嘧啶环(6C 环)的暗态 DNA Ag 纳米团簇(NC)。有趣的是,暗态 DNA Ag NCs 可以被点亮以显示强红色发射纳米团簇。基于这些令人兴奋的发现,我们创建了一个前所未有的升级型开启生物传感系统[熵驱动催化电路(EDCC)-Ag NCs/氧化石墨烯(GO)],该系统利用 EDCC 精确地操纵 DNA Ag NCs 在 GO 表面从吸附到解吸的构象转变。得益于 GO 的有效猝灭和 EDCC 的信号放大能力,新开发的 EDCC-Ag NCs/GO 生物传感系统具有高信号背景比(26 倍)和灵敏度(低至 0.4 pM 的检测限)。同时,它在缓冲液和生物样品中具有良好的特异性、出色的稳定性和可靠性。据我们所知,这是第一个采用 EDCC 精确调节 DNA Ag NCs 在 GO 表面的构象转变以获得具有低背景、强荧光、高对比度和灵敏度的生物传感器的例子。这一令人兴奋的发现可能为基于发夹模板 DNA Ag NCs 的新型开启型生物传感器在光学成像和生物分析领域的构建提供了新途径。

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