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基于 4-巯基吡啶功能化的银纳米粒子的反聚集作用的超灵敏表面增强拉曼散射检测胰蛋白酶:一种用于蛋白酶的光学传感平台。

Ultrasensitive surface-enhanced Raman scattering detection of trypsin based on anti-aggregation of 4-mercaptopyridine-functionalized silver nanoparticles: an optical sensing platform toward proteases.

机构信息

Key Laboratory of Coastal Zone Environmental Processes and Ecological Remediation, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003, PR China.

出版信息

Nanoscale. 2013 Jul 7;5(13):5905-11. doi: 10.1039/c3nr00637a. Epub 2013 May 24.

Abstract

In this work, a simple and sensitive surface-enhanced Raman scattering (SERS) strategy was developed for recognition and detection of trypsin, by using anti-aggregation of 4-mercaptopyridine (4-MPY)-functionalized silver nanoparticles (AgNPs) based on the interaction between protamine and trypsin. The polycationic protamine not only served as a substrate for enzyme hydrolysis but also worked as a medium for SERS enhancement, which could bind negatively charged 4-MPY-functionalized AgNPs and induce their aggregation. The hydrolysis catalyzed with trypsin in sample solution decreased the concentration of free protamine, resulting in the dispersion of AgNPs and thus decreasing the Raman intensity of 4-MPY, by which the trypsin could be sensed optically. A detection level down to 0.1 ng mL(-1) for trypsin was obtained. The induced accumulation of AgNPs modified with Raman reporter 4-MPY largely enhanced the SERS responses. A good linearity was found within the wide range over five orders of magnitude and reasonable relative standard deviations (between 2.4 and 11.6%) were attained. By using trypsin as a model, the new concept can provide an excellent platform for ultrasensitive SERS measurements of various proteases/enzymes which can lead to nanoparticles stability change through catalyzed hydrolysis toward substrate.

摘要

在这项工作中,开发了一种简单灵敏的表面增强拉曼散射(SERS)策略,用于识别和检测胰蛋白酶,方法是利用基于鱼精蛋白与胰蛋白酶相互作用的 4-巯基吡啶(4-MPY)功能化银纳米粒子(AgNPs)的聚集。多正电荷的鱼精蛋白不仅用作酶水解的底物,而且还用作 SERS 增强的介质,它可以结合带负电荷的 4-MPY 功能化 AgNPs 并诱导它们聚集。在样品溶液中,胰蛋白酶催化的水解反应降低了游离鱼精蛋白的浓度,导致 AgNPs 分散,从而降低了 4-MPY 的拉曼强度,从而可以通过光学检测到胰蛋白酶。对胰蛋白酶的检测下限低至 0.1 ng mL(-1)。与拉曼报告分子 4-MPY 修饰的 AgNPs 的诱导聚集大大增强了 SERS 响应。在五个数量级的宽范围内发现了良好的线性关系,并且获得了合理的相对标准偏差(在 2.4%至 11.6%之间)。通过使用胰蛋白酶作为模型,该新概念可以为各种蛋白酶/酶的超灵敏 SERS 测量提供极好的平台,这些蛋白酶/酶可以通过对底物的催化水解导致纳米粒子稳定性变化。

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