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利用磁场定向定位的单分子荧光法检测 DNA 纳米颗粒的泽特定摩尔级。

Zeptomole detection of DNA nanoparticles by single-molecule fluorescence with magnetic field-directed localization.

机构信息

Department of Chemistry and Biochemistry, University of Texas at Austin, Austin, TX 78712, USA.

出版信息

Anal Biochem. 2012 Dec 1;431(1):40-7. doi: 10.1016/j.ab.2012.08.017. Epub 2012 Aug 26.

DOI:10.1016/j.ab.2012.08.017
PMID:22929698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3478425/
Abstract

Single-molecule fluorescence methods offer the promise of ultrasensitive detection of biomolecules, but the passive immobilization methods commonly employed require analyte concentrations in the picomolar range. Here, we demonstrate that superparamagnetic Fe(3)O(4) nanoparticles (NPs) can be used with an external magnetic field as a simple strategy to enhance the immobilization efficiency and thereby decrease the detection limit. Inorganic NPs functionalized with streptavidin were bound to biotinylated single-stranded DNA oligonucleotides, which were in turn annealed to complementary oligonucleotides labeled with a Cy3 fluorescent dye. Using an external magnetic field, the superparamagnetic nanoparticles were localized to a specific region within the flow chamber surface. From the single-molecule fluorescence time traces, single-step photobleaching indicated that the surface-immobilized NPs were primarily bound with a single Cy3-labeled oligonucleotide. This strategy gave a concentration detection limit for the Cy3-labeled oligonucleotide of 100aM, 3000-fold lower than that from an analogous strategy with passive immobilization. With a sample volume of 25μl, this method achieved a mole detection limit of approximately 2.5zmol (∼1500 molecules). Together, the results support that idea that single-molecule fluorescence methods could be used for biological applications such as detection and measurements of nucleic acids from biological or clinical samples without polymerase chain reaction amplification.

摘要

单分子荧光方法有望实现对生物分子的超高灵敏度检测,但常用的被动固定化方法需要分析物浓度达到皮摩尔级。在这里,我们证明超顺磁 Fe(3)O(4) 纳米粒子 (NPs) 可以与外部磁场一起用作一种简单的策略来提高固定化效率,从而降低检测限。用链霉亲和素功能化的无机 NPs 与生物素化的单链 DNA 寡核苷酸结合,然后寡核苷酸与用 Cy3 荧光染料标记的互补寡核苷酸退火。通过外部磁场,超顺磁纳米粒子被定位到流动室表面的特定区域。从单分子荧光时间轨迹可以看出,单步光漂白表明表面固定化的 NPs 主要与单个 Cy3 标记的寡核苷酸结合。与具有被动固定化的类似策略相比,这种策略使 Cy3 标记的寡核苷酸的浓度检测限达到 100aM,降低了 3000 倍。在 25μl 的样品体积下,该方法的摩尔检测限约为 2.5zmol(约 1500 个分子)。总之,这些结果表明,单分子荧光方法可用于生物应用,例如无需聚合酶链反应扩增即可从生物或临床样本中检测和测量核酸。

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