Issue 5, 2016

Oriented assembly of invisible probes: towards single mRNA imaging in living cells

Abstract

Due to the complexity of biological systems and the ultralow concentration of analytes, improving the signal-to-noise ratio and lowering the limit of detection to allow highly sensitive detection is key to biomolecule analysis, especially intracellular analysis. Here, we present a method for highly sensitive imaging of mRNA in living cells by using novel invisible oriented probes to construct a turn-on signal generation mechanism from zero background. Two DNA probes (S1 and S2) are asymmetrically modified on two small gold nanoparticles (AuNPs) with a diameter of 20 nm. The hybridization of the two DNA probes with a single target mRNA leads to the formation of an AuNP dimer which shows a prominent plasmonic coupling effect. It generates a strong scattering signal from zero-background under a dark-field spectral analysis system. The unique design of the oriented assembly dimer has the ability to easily discriminate the target signal from the inherent cellular background noise in intracellular detection, thus making this approach a valuable technique for imaging single survivin mRNA and monitoring the distribution of survivin mRNA in tumor cells.

Graphical abstract: Oriented assembly of invisible probes: towards single mRNA imaging in living cells

Supplementary files

Article information

Article type
Edge Article
Submitted
16 Nov 2015
Accepted
04 Feb 2016
First published
04 Feb 2016
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2016,7, 3256-3263

Oriented assembly of invisible probes: towards single mRNA imaging in living cells

X. Li, Z. Zhang, W. Zhao, X. Xia, J. Xu and H. Chen, Chem. Sci., 2016, 7, 3256 DOI: 10.1039/C5SC04369G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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