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使用体积扩增磁性纳米珠的灵敏分子诊断方法。

Sensitive molecular diagnostics using volume-amplified magnetic nanobeads.

作者信息

Strömberg Mattias, Göransson Jenny, Gunnarsson Klas, Nilsson Mats, Svedlindh Peter, Strømme Maria

机构信息

Department of Engineering Sciences, Division of Nanotechnology and Functional Materials, Uppsala University, The Angström Laboratory, Box 534, SE-751 21 Uppsala, Sweden.

出版信息

Nano Lett. 2008 Mar;8(3):816-21. doi: 10.1021/nl072760e. Epub 2008 Feb 2.

Abstract

In this letter, we demonstrate a new principle for diagnostics based on DNA sequence detection using single-stranded oligonucleotide tagged magnetic nanobeads. The target DNA is recognized and volume-amplified to large coils by circularization of linear padlock probes through probe hybridization and ligation, followed by rolling circle amplification (RCA). Upon hybridization of the nanobeads in the RCA coils, the complex magnetization spectrum of the beads changes dramatically, induced by the attached volume-amplified target molecules. We show that the magnetization spectrum of the nanobeads can be used for concentration determination of RCA coils down to the pM range, thus creating the opportunity for nonfluorescence-based cost-efficient high-sensitivity diagnostics tool. We also show that the bead incorporation in the coils is diffusion-controlled and consequently may be accelerated by incubating the sample at higher temperatures.

摘要

在本信函中,我们展示了一种基于使用单链寡核苷酸标记磁纳米珠进行DNA序列检测的诊断新原理。通过线性锁式探针的环化(通过探针杂交和连接),随后进行滚环扩增(RCA),目标DNA被识别并体积扩增为大的环状分子。在纳米珠与RCA环状分子杂交后,由于附着的体积扩增目标分子的作用,纳米珠的复合磁化光谱会发生显著变化。我们表明,纳米珠的磁化光谱可用于测定低至pM范围的RCA环状分子的浓度,从而为基于非荧光的经济高效高灵敏度诊断工具创造了机会。我们还表明,纳米珠在环状分子中的掺入是扩散控制的,因此可以通过在更高温度下孵育样品来加速。

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