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Characterization of Binding of Magnetic Nanoparticles to Rolling Circle Amplification Products by Turn-On Magnetic Assay

机译:磁性纳米颗粒与滚环扩增产物的结合特性通过开启磁性分析

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摘要

The specific binding of oligonucleotide-tagged 100 nm magnetic nanoparticles (MNPs) to rolling circle products (RCPs) is investigated using our newly developed differential homogenous magnetic assay (DHMA). The DHMA measures ac magnetic susceptibility from a test and a control samples simultaneously and eliminates magnetic background signal. Therefore, the DHMA can reveal details of binding kinetics of magnetic nanoparticles at very low concentrations of RCPs. From the analysis of the imaginary part of the DHMA signal, we find that smaller MNPs in the particle ensemble bind first to the RCPs. When the RCP concentration increases, we observe the formation of agglomerates, which leads to lower number of MNPs per RCP at higher concentrations of RCPs. The results thus indicate that a full frequency range of ac susceptibility observation is necessary to detect low concentrations of target RCPs and a long amplification time is not required as it does not significantly increase the number of MNPs per RCP. The findings are critical for understanding the underlying microscopic binding process for improving the assay performance. They furthermore suggest DHMA is a powerful technique for dynamically characterizing the binding interactions between MNPs and biomolecules in fluid volumes.
机译:使用我们新开发的差异均质磁检测法(DHMA),研究了寡核苷酸标记的100 nm磁性纳米颗粒(MNP)与滚环产物(RCP)的特异性结合。 DHMA同时测量来自测试和对照样品的交流磁化率,并消除了磁性背景信号。因此,DHMA可以揭示在非常低的RCP浓度下磁性纳米颗粒的结合动力学细节。通过分析DHMA信号的虚部,我们发现粒子集合中的较小MNP首先与RCP绑定。当RCP浓度增加时,我们观察到附聚物的形成,这导致在较高RCP浓度下每个RCP的MNP数量减少。结果因此表明,要检测低浓度的目标RCP,必须有整个频率范围的磁化率观测,并且不需要很长的扩增时间,因为它不会显着增加每个RCP的MNP数量。这些发现对于理解潜在的微观结合过程以提高测定性能至关重要。他们进一步认为,DHMA是动态表征流体体积中MNP与生物分子之间结合相互作用的强大技术。

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