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荧光探针包被在亲和素蛋白中以消除血清中非特异性荧光并提高检测灵敏度。

Fluorescent Probe Encapsulated in Avidin Protein to Eliminate Nonspecific Fluorescence and Increase Detection Sensitivity in Blood Serum.

机构信息

Department of Chemistry, National Tsing Hua University , 101 Section 2, Kuang Fu Road, Hsinchu 30013, Taiwan, Republic of China.

Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing Hua University , 101 Section 2, Kuang Fu Road, Hsinchu 30013, Taiwan, Republic of China.

出版信息

Anal Chem. 2016 Aug 16;88(16):7873-7. doi: 10.1021/acs.analchem.6b02111. Epub 2016 Jul 26.

Abstract

Quantitative detection of trace amounts of a biomarker in protein rich human blood plasma using fluorescent probes is a great challenge as the real signal is usually obscured by nonspecific fluorescence. This problem occurs because most of the fluorescent dyes bind very tightly with blood proteins to produce a large fluorescence increase, resulting in overestimation of the biomarker concentrations and false positive diagnosis. In this paper, we report that biotinylated fluorescent probes encapsulated in avidin protein can generate very specific fluorescence in blood serum by blocking out nonspecific dye-protein interactions. We applied our novel probe design to detect two different types of biomolecules, hydrogen sulfide and nitroreductase. Our Avidin conjugated probes achieved quantitative analyte detection in blood serum; whereas concentrations were overestimated up to 320-fold when bare fluorescent probes were employed. As compared to conventional approaches where fluorescent probes are encapsulated into polymers and nanoparticles, our simple approach successfully overcomes many key issues such as dye leakage, long preparation steps, inconsistent dye-host ratios, difficulty in constructing in situ in a complex medium, and limited application to detect only small metabolites.

摘要

使用荧光探针定量检测富含蛋白质的人血浆中的痕量生物标志物是一项巨大的挑战,因为真实信号通常被非特异性荧光所掩盖。这个问题的出现是因为大多数荧光染料与血液蛋白结合非常紧密,产生大量的荧光增强,从而导致生物标志物浓度的高估和假阳性诊断。在本文中,我们报告说,生物素化荧光探针封装在亲和素蛋白中,可以通过阻断非特异性染料-蛋白相互作用在血清中产生非常特异性的荧光。我们将我们的新型探针设计应用于检测两种不同类型的生物分子,硫化氢和硝基还原酶。我们的亲和素偶联探针在血清中实现了定量分析物检测;而当使用裸荧光探针时,浓度被高估了多达 320 倍。与荧光探针被封装在聚合物和纳米颗粒中的传统方法相比,我们的简单方法成功克服了许多关键问题,如染料泄漏、繁琐的制备步骤、染料-宿主比例不一致、在复杂介质中构建原位的困难以及应用受限,只能检测到少量代谢物。

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