DNA甲基化
DNA
纳米技术
材料科学
计算生物学
化学
生物
生物物理学
遗传学
基因
基因表达
作者
Xiaoyin Sun,Takao Yasui,Takeshi Yanagida,Noritada Kaji,Sakon Rahong,Masaki Kanai,Kazuki Nagashima,Tomoji Kawai,Yoshinobu Baba
标识
DOI:10.1080/14686996.2016.1223516
摘要
DNA methylation is a stable epigenetic modification, which is well known to be involved in gene expression regulation. In general, however, analyzing DNA methylation requires rather time consuming processes (24-96 h) via DNA replication and protein modification. Here we demonstrate a methodology to analyze DNA methylation at a single DNA molecule level without any protein modifications by measuring the contracted length and relaxation time of DNA within a nanochannel. Our methodology is based on the fact that methylation makes DNA molecules stiffer, resulting in a longer contracted length and a longer relaxation time (a slower contraction rate). The present methodology offers a promising way to identify DNA methylation without any protein modification at a single DNA molecule level within 2 h.
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