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基于羧基化石墨相氮化碳作为发光体的大豆凝集素电化学发光生物传感器。

An electrochemiluminescence biosensor for the detection of soybean agglutinin based on carboxylated graphitic carbon nitride as luminophore.

机构信息

Key Laboratory of Luminescence and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, China.

Institute of Materials Science & Devices, Suzhou University of Science and Technology, Suzhou, 215009, China.

出版信息

Anal Bioanal Chem. 2019 Sep;411(23):6049-6056. doi: 10.1007/s00216-019-01986-w. Epub 2019 Jul 6.

Abstract

As an important glycoprotein of the lectin family, soybean agglutinin (SBA) is an anti-nutritional factor with considerable toxic and side effects and plays a significant role in tumor analysis. In order to achieve the sensitive detection of SBA, a sandwich-structured electrochemiluminescence (ECL) biosensor was constructed using carboxylated carbon nitride (C-g-CN) as luminophore and D-galactosamine (galM) as a recognition element. A glassy carbon electrode (GCE) was modified with Au nanoparticles (Au NPs) for capturing the galM via Au-N bond, and further capturing the target SBA by specific recognition between galM and SBA. In the presence of SBA, the composite C-g-CN-galM was immobilized onto the electrode. With the increase in the concentration of SBA, the ECL signal from C-g-CN increased, thus achieving a signal-on detection of SBA. The linear range of the biosensor was 1.0 ng/mL~10 μg/mL and detection limit for SBA was as low as 0.33 ng/mL. In this construction strategy, C-g-CN not only acted as an excellent signal probe, but also as an immobilization matrix to easily achieve a high loading of the small molecule recognition element galM. This strategy provides a simple alternative SBA detection platform. Graphical abstract.

摘要

作为凝集素家族的一种重要糖蛋白,大豆凝集素(SBA)是一种具有相当毒性和副作用的抗营养因子,在肿瘤分析中发挥着重要作用。为了实现 SBA 的灵敏检测,构建了一种夹心结构的电化学发光(ECL)生物传感器,使用羧基化氮化碳(C-g-CN)作为发光体和 D-半乳糖胺(galM)作为识别元件。玻碳电极(GCE)经金纳米粒子(Au NPs)修饰,通过 Au-N 键捕获 galM,并通过 galM 与 SBA 之间的特异性识别进一步捕获靶标 SBA。在存在 SBA 的情况下,复合 C-g-CN-galM 被固定在电极上。随着 SBA 浓度的增加,C-g-CN 的 ECL 信号增加,从而实现了 SBA 的信号开启检测。该生物传感器的线性范围为 1.0 ng/mL~10 μg/mL,检测 SBA 的检测限低至 0.33 ng/mL。在这种构建策略中,C-g-CN 不仅充当了优异的信号探针,还充当了固定化基质,可轻松实现小分子识别元件 galM 的高负载。该策略为 SBA 检测提供了一种简单的替代平台。

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