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利用金纳米粒子在纳摩尔水平下对糖蛋白进行无标记检测的凝集素生物传感器。

Label-free detection of glycoproteins by the lectin biosensor down to attomolar level using gold nanoparticles.

机构信息

Department of Glycobiotechnology, Institute of Chemistry, Slovak Academy of Sciences, Dúbravská cesta 9, 845 38 Bratislava, Slovak Republic.

出版信息

Talanta. 2013 Apr 15;108:11-8. doi: 10.1016/j.talanta.2013.02.052. Epub 2013 Mar 1.

Abstract

We present here an ultrasensitive electrochemical biosensor based on a lectin biorecognition capable to detect concentrations of glycoproteins down to attomolar (aM) level by investigation of changes in the charge transfer resistance (Rct) using electrochemical impedance spectroscopy (EIS). On polycrystalline gold modified by an aminoalkanethiol linker layer, gold nanoparticles were attached. A Sambucus nigra agglutinin was covalently immobilised on a mixed self-assembled monolayer formed on gold nanoparticles and finally, the biosensor surface was blocked by poly(vinyl alcohol). The lectin biosensor was applied for detection of sialic acid containing glycoproteins fetuin and asialofetuin. Building of a biosensing interface was carefully characterised by a broad range of techniques such as electrochemistry, EIS, atomic force microscopy, scanning electron microscopy and surface plasmon resonance with the best performance of the biosensor achieved by application of HS-(CH2)11-NH2 linker and gold nanoparticles with a diameter of 20 nm. The lectin biosensor responded to an addition of fetuin (8.7% of sialic acid) with sensitivity of (338 ± 11) Ω decade(-1) and to asialofetuin (≤ 0.5% of sialic acid) with sensitivity of (109 ± 10) Ω decade(-1) with a blank experiment with oxidised asialofetuin (without recognisable sialic acid) revealing sensitivity of detection of (79 ± 13) Ω decade(-1). These results suggest the lectin biosensor responded to changes in the glycan amount in a quantitative way with a successful validation by a lectin microarray. Such a biosensor device has a great potential to be employed in early biomedical diagnostics of diseases such as arthritis or cancer, which are connected to aberrant glycosylation of protein biomarkers in biological fluids.

摘要

我们在此提出了一种基于凝集素生物识别的超灵敏电化学生物传感器,该传感器能够通过使用电化学阻抗谱(EIS)研究电荷转移电阻(Rct)的变化来检测浓度低至飞摩尔(aM)级别的糖蛋白。在经过氨基烷硫醇连接层修饰的多晶金上,附着了金纳米粒子。桑椹凝集素通过共价固定在形成于金纳米粒子上的混合自组装单层上,最后,生物传感器表面通过聚乙烯醇封闭。该凝集素生物传感器用于检测含有唾液酸的糖蛋白胎球蛋白和去唾液酸胎球蛋白。通过广泛的技术,如电化学、EIS、原子力显微镜、扫描电子显微镜和表面等离子体共振对生物传感界面的构建进行了仔细的表征,其中生物传感器的最佳性能是通过应用 HS-(CH2)11-NH2 连接体和直径为 20nm 的金纳米粒子实现的。该凝集素生物传感器对胎球蛋白(含 8.7%唾液酸)的添加有响应,灵敏度为(338±11)Ω decade(-1),对去唾液酸胎球蛋白(含≤0.5%唾液酸)的添加有响应,灵敏度为(109±10)Ω decade(-1),而氧化的去唾液酸胎球蛋白(不含可识别的唾液酸)的空白实验显示检测灵敏度为(79±13)Ω decade(-1)。这些结果表明,该凝集素生物传感器能够以定量的方式响应聚糖数量的变化,并通过凝集素微阵列成功验证。这种生物传感器设备在关节炎或癌症等疾病的早期生物医学诊断中具有很大的应用潜力,这些疾病与生物体液中蛋白质生物标志物的异常糖基化有关。

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