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J Nanobiotechnology. 2018 Oct 9;16(1):78. doi: 10.1186/s12951-018-0407-5.

A resonance Rayleigh scattering sensor for sensitive differentiation of telomere DNA length and monitoring special motifs (G-quadruplex and i-motif) based on the Ag nanoclusters and NAND logic gate responding to chemical input signals.

Wang S1,2, Qu F3, Han W4, You J1,5.

Author information

1
The Key Laboratory of Life-Organic Analysis, Qufu Normal University, Qufu, 273165, Shandong, China.
2
The Key Laboratory for Colloid and Interface Chemistry of Education Ministry, Shandong University, Jinan, 250100, Shandong, China.
3
The Key Laboratory of Life-Organic Analysis, Qufu Normal University, Qufu, 273165, Shandong, China. qufei3323@163.com.
4
Laboratory Animal Center, Chongqing Medical University, Chongqing, China.
5
Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, 810001, China.

Abstract

BACKGROUND:

Differentiation of telomere length is of vital importance because telomere length is closely related with several deadly diseases such as cancer. Additionally, G-quadruplex and i-motif formation in telomeric DNA have been shown to act as a negative regulator of telomere elongation by telomerase in vivo and are considered as an attractive drug target for cancer chemotherapy.

RESULTS:

In this assay, Ag nanoclusters templated by hyperbranched polyethyleneimine (PEI-Ag NCs) are designed as a new novel resonance Rayleigh scattering (RRS) probe for sensitive differentiation of telomere length and monitoring special motifs (G-quadruplex and i-motif). In this assay, free PEI-Ag NC probe or DNA sequence alone emits low intensities of RRS, while the formation of PEI-Ag NCs/DNA complexes yields greatly enhanced RRS signals; however, when PEI-Ag NCs react with G-quadruplex or i-motif, the intensities of RRS exhibit slight changes. At the same concentration, the enhancement of RRS signal is directly proportional to the length of telomere, and the sensitivity of 64 bases is the highest with the linear range of 0.3-50 nM (limit of detection 0.12 nM). On the other hand, due to the conversion of telomere DNA molecules among multiple surrounding conditions, a DNA logic gate is developed on the basis of two chemical input signals (K+ and H+) and a change in RRS intensity as the output signal.

CONCLUSION:

Our results indicate that PEI-Ag NCs can serve as a novel RRS probe to identify DNA length and monitor G-quadruplex/i-motif through the different increasing degrees of RRS intensity. Meanwhile, the novel attributes of the nanoprobe stand superior to those involving dyes or labeled DNA because of no chemical modification, low cost, green, and high efficiency.

KEYWORDS:

Ag nanoclusters; DNA logic gate; G-quadruplex; Telomere DNA length; i-motif

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