The Spherical Nucleic Acids mRNA Detection Paradox

R. Lévy, M. Held, D. Mason, Joan Comenge, G. Carolan
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引用次数: 10

Abstract

From the 1950s onwards, our understanding of the formation and intracellular trafficking of membrane vesicles was informed by experiments in which cells were exposed to gold nanoparticles and their uptake and localisation, studied by electron microscopy.  In the last decade, building on progress in the synthesis of gold nanoparticles and their controlled functionalisation with a large variety of biomolecules (DNA, peptides, polysaccharides), new applications have been proposed, including the imaging and sensing of intracellular events. Yet, as already demonstrated in the 1950s, uptake of nanoparticles results in confinement within an intracellular vesicle which in principle should preclude sensing of cytosolic events. To study this apparent paradox, we focus on a commercially available nanoparticle probe that detects mRNA through the release of a fluorescently-labelled oligonucleotide (unquenching the fluorescence) in the presence of the target mRNA. Using electron, fluorescence and photothermal microscopy, we show that the probes remain in endocytic compartments and that they do not report on mRNA level. We suggest that the validation of any nanoparticle-based probes for intracellular sensing should include a quantitative and thorough demonstration that the probes can reach the cytosolic compartment.
球形核酸mRNA检测悖论
从20世纪50年代开始,我们对膜囊泡的形成和细胞内运输的理解是通过电子显微镜研究细胞暴露于金纳米颗粒及其摄取和定位的实验得到的。在过去的十年中,基于金纳米颗粒的合成及其与多种生物分子(DNA,肽,多糖)的控制功能化的进展,已经提出了新的应用,包括细胞内事件的成像和传感。然而,正如20世纪50年代已经证明的那样,纳米颗粒的摄取导致细胞内囊泡的限制,原则上应该排除对细胞质事件的感知。为了研究这个明显的悖论,我们重点研究了一种市售的纳米颗粒探针,该探针通过在目标mRNA存在的情况下释放荧光标记的寡核苷酸(不猝灭荧光)来检测mRNA。使用电子、荧光和光热显微镜,我们发现探针留在内吞室中,并且它们不报告mRNA水平。我们建议,任何基于纳米粒子的细胞内传感探针的验证都应该包括一个定量和彻底的证明,即探针可以到达细胞质室。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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