Issue 9, 2022

Single polymeric microfiber waveguide platform for sensitive detection and discrimination of DNA methylation

Abstract

The development of a rapid and sensitive detection platform for DNA and DNA methylation in complex biological environments has attracted considerable attention. Herein, we describe a detection platform for p16 and p16 methylation in buffer and serum based on a single polymeric fluorescent microfiber waveguide with sandwich-structured hybridization designs. The target p16 could be captured by oligonucleotides conjugated on the surface of polymeric microfibers and oligonucleotides conjugated with gold nanoparticles, resulting in quenching the out-coupled tip emission of the microfiber waveguide. Then the restriction digestion enzyme HpaII was applied to specifically recognize the unmethylated 5′-CCGG-3′ site and cut the formed sandwich structure. The gold nanoparticles could be removed from the surface of chitosan fiber so that the out-coupled tip emission of the polymeric fluorescent microfiber would be partially recovered. It is noteworthy that the proposed polymeric microfiber waveguide platform exhibited selective and sensitive detection of p16 with a low limit of 2 pM and excellent analytical performance of methylation as low as 5% difference. This strategy avoids the use of traditional PCR-based amplification and tedious operative processes, and we envisage that this technique could be extended to various DNA methylation analyses, which is meaningful for early clinical diagnosis of diseases.

Graphical abstract: Single polymeric microfiber waveguide platform for sensitive detection and discrimination of DNA methylation

Supplementary files

Article information

Article type
Paper
Submitted
11 Dec 2021
Accepted
14 Mar 2022
First published
15 Mar 2022

Analyst, 2022,147, 1892-1898

Single polymeric microfiber waveguide platform for sensitive detection and discrimination of DNA methylation

K. Yang, X. Feng, G. Yu, W. Han, F. Liu, Y. Xie, H. Zhang, Y. Yu and G. Zou, Analyst, 2022, 147, 1892 DOI: 10.1039/D1AN02243A

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