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手性等离子体纳米金字塔自组装的金和上转换纳米粒子用于活细胞中 microRNA 的双模超灵敏定量分析

Dual-Mode Ultrasensitive Quantification of MicroRNA in Living Cells by Chiroplasmonic Nanopyramids Self-Assembled from Gold and Upconversion Nanoparticles.

机构信息

State Key Lab of Food Science and Technology, International Joint Research Laboratory for Biointerface and Biodetection, School of Food Science and Technology, Jiangnan University , Wuxi, Jiangsu 214122, People's Republic of China.

Department of Chemical Engineering, University of Michigan , Ann Arbor, Michigan 48109-2136, United States.

出版信息

J Am Chem Soc. 2016 Jan 13;138(1):306-12. doi: 10.1021/jacs.5b10309. Epub 2015 Dec 29.

Abstract

Chiral self-assembled nanomaterials with biological applications have attracted great interest. In this study, DNA-driven gold-upconversion nanoparticle (Au-UCNP) pyramids were fabricated to detect intracellular microRNA (miRNA) in real time. The Au-UCNP pyramids are doubly optically active, displaying strong plasmonic circular dichroism (CD) at 521 nm and significant luminescence in 500-600 nm, and therefore can be monitored by both of them. CD will decrease while the luminescence intensity increases in the presence of miRNA. The experimental results show that the CD intensity had an outstanding linear range from 0.073 to 43.65 fmol/10 μg(RNA) and a limit of detection (LOD) of 0.03 fmol/10 μg(RNA), whereas the luminescence intensity ranged from 0.16 to 43.65 fmol/10 μg(RNA) with a LOD of 0.12 fmol/10 μg(RNA). These data indicate that the CD signal is much more sensitive to the concentration of miRNA than the luminescent signal, which is attributed to the strong CD intensity arising from the spin angular momentum of the photon interaction with chiral nanostructures and the plasmonic enhancement of the intrinsic chirality of DNA molecules in the pyramids. This approach opens up a new avenue to the ultrasensitive detection and quantification of miRNA in living cells.

摘要

具有生物应用的手性自组装纳米材料引起了极大的关注。在这项研究中,我们制备了 DNA 驱动的金上转换纳米粒子(Au-UCNP)金字塔,以实时检测细胞内 microRNA(miRNA)。Au-UCNP 金字塔具有双重光学活性,在 521nm 处显示出强的等离子体圆二色性(CD),在 500-600nm 处显示出显著的发光,因此可以通过它们两者来监测。在存在 miRNA 的情况下,CD 强度会降低,而发光强度会增加。实验结果表明,CD 强度在 0.073 至 43.65fmol/10μg(RNA)之间具有出色的线性范围和 0.03fmol/10μg(RNA)的检测限(LOD),而发光强度在 0.16 至 43.65fmol/10μg(RNA)之间,检测限(LOD)为 0.12fmol/10μg(RNA)。这些数据表明,CD 信号对 miRNA 浓度的灵敏度远高于发光信号,这归因于光子与手性纳米结构相互作用的自旋角动量引起的强 CD 强度以及金字塔中 DNA 分子固有手性的等离子体增强。该方法为在活细胞中对 miRNA 进行超灵敏检测和定量开辟了新途径。

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