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Harnessing immunomagnetic separation and quantum dot-based quantification capacities for the enumeration of absolute levels of biomarker

机译:利用免疫磁分离和基于量子点的定量能力来枚举生物标志物的绝对水平

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摘要

The field of biomarker quantification has experienced a growth parallel to the discovery of new materials. In this paper, we propose an innovative system for the separation and quantification of biomarkers using a simple magnetic bead (MB)-quantum dot (QD) sandwich assay. The basis of the system lies in the interaction between histidine residues on protein G and Ni ions on QDs, and the use of imidazole to selectively detach QDs bound to target biomarkers, in effect enumerating the absolute number of biomarker units. We used C-reactive protein (CRP) as a proof-of-concept and demonstrated a detection sensitivity of 82.5 fmoles in 50 μl of sample volume, a commonly used analytical volume (e.g. ELISA). Although CRP was used as a model to conduct this study, the sensitivity and simplicity of this detachable system make it a viable approach in the quantification of other target analytes.
机译:生物标志物定量化领域经历了与发现新材料平行的增长。在本文中,我们提出了一种使用简单的磁珠(MB)-量子点(QD)夹心测定法对生物标志物进行分离和定量的创新系统。该系统的基础在于蛋白质G上的组氨酸残基与QD上的Ni离子之间的相互作用,以及使用咪唑选择性地分离与靶标生物标志物结合的QD,从而有效地枚举了生物标志物单元的绝对数量。我们使用C反应蛋白(CRP)作为概念验证,并证明了在50μl样品体积(常用的分析体积)(例如ELISA)中的检测灵敏度为82.5 fmoles。尽管CRP被用作进行这项研究的模型,但这种可分离系统的灵敏性和简便性使其成为定量其他目标分析物的可行方法。

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