Selective adsorption of unmethylated DNA on ZnO nanowires for separation of methylated DNA.

IF 6.1 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Lab on a Chip Pub Date : 2025-01-10 DOI:10.1039/d4lc00893f
Marina Musa, Zetao Zhu, Hiromi Takahashi, Wataru Shinoda, Yoshinobu Baba, Takao Yasui
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Abstract

DNA methylation is a crucial epigenetic modification used as a biomarker for early cancer progression. However, existing methods for DNA methylation analysis are complex, time-consuming, and prone to DNA degradation. This work demonstrates selective capture of unmethylated DNAs using ZnO nanowires without chemical or biological modifications, thereby concentrating methylated DNA, particularly those with high methylation levels that can predict cancer risk. We observe varying affinities between methylated and unmethylated DNA on ZnO nanowires, which may be influenced by differences in hydrogen bonding strength, potentially related to the effects of methylation on DNA strand behavior, including self-aggregation and stretching inhibition. As a result, the nanowire-based microfluidic device effectively collects unmethylated DNA, leading to a significantly increased ratio of methylated to unmethylated DNA, particularly for collecting low-concentration methylated DNA. This simplified microfluidic device, composed of ZnO nanowires, enables direct separation of specific methylated DNA, offering a potential approach for DNA methylation mapping in clinical disease diagnostics.

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未甲基化DNA在ZnO纳米线上选择性吸附分离甲基化DNA。
DNA甲基化是一种重要的表观遗传修饰,被用作早期癌症进展的生物标志物。然而,现有的DNA甲基化分析方法复杂,耗时,并且容易导致DNA降解。这项工作证明了使用ZnO纳米线在没有化学或生物修饰的情况下选择性捕获非甲基化DNA,从而集中甲基化DNA,特别是那些可以预测癌症风险的高甲基化水平的DNA。我们观察到甲基化和未甲基化的DNA在ZnO纳米线上的亲合力不同,这可能受到氢键强度差异的影响,可能与甲基化对DNA链行为的影响有关,包括自聚集和拉伸抑制。因此,基于纳米线的微流控装置有效地收集了未甲基化的DNA,导致甲基化与非甲基化DNA的比例显着增加,特别是在收集低浓度甲基化DNA时。这种由ZnO纳米线组成的简化微流控装置可以直接分离特定的甲基化DNA,为临床疾病诊断中的DNA甲基化定位提供了一种潜在的方法。
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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来源期刊
Lab on a Chip
Lab on a Chip 工程技术-化学综合
CiteScore
11.10
自引率
8.20%
发文量
434
审稿时长
2.6 months
期刊介绍: Lab on a Chip is the premiere journal that publishes cutting-edge research in the field of miniaturization. By their very nature, microfluidic/nanofluidic/miniaturized systems are at the intersection of disciplines, spanning fundamental research to high-end application, which is reflected by the broad readership of the journal. Lab on a Chip publishes two types of papers on original research: full-length research papers and communications. Papers should demonstrate innovations, which can come from technical advancements or applications addressing pressing needs in globally important areas. The journal also publishes Comments, Reviews, and Perspectives.
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