Suppr超能文献

基于合成分子/蛋白质杂合探针的 DNA 甲基化的活细胞成像

Live-Cell Imaging of DNA Methylation Based on Synthetic-Molecule/Protein Hybrid Probe.

机构信息

Graduate School of Engineering, Osaka University Suita, Osaka, 565-0871, Japan.

Immunology Fontier Research Center, Osaka University Suita, Osaka, 565-0871, Japan.

出版信息

Chem Rec. 2018 Dec;18(12):1672-1680. doi: 10.1002/tcr.201800039. Epub 2018 Jun 4.

Abstract

The epigenetic modification of DNA involves the conversion of cytosine to 5-methylcytosine, also known as DNA methylation. DNA methylation is important in modulating gene expression and thus, regulating genome and cellular functions. Recent studies have shown that aberrations in DNA methylation are associated with various epigenetic disorders or diseases including cancer. This stimulates great interest in the development of methods that can detect and visualize DNA methylation. For instance, fluorescent proteins (FPs) in conjugation with methyl-CpG-binding domain (MBD) have been employed for live-cell imaging of DNA methylation. However, the FP-based approach showed fluorescence signals for both the DNA-bound and -unbound states and thus differentiation between these states is difficult. Synthetic-molecule/protein hybrid probes can provide an alternative to overcome this restriction. In this article, we discuss the synthetic-molecule/protein hybrid probe that we developed recently for live-cell imaging of DNA methylation, which exhibited fluorescence enhancement only after binding to methylated DNA.

摘要

DNA 的表观遗传修饰涉及胞嘧啶向 5-甲基胞嘧啶的转化,也称为 DNA 甲基化。DNA 甲基化在调节基因表达中很重要,从而调节基因组和细胞功能。最近的研究表明,DNA 甲基化的异常与各种表观遗传障碍或疾病有关,包括癌症。这激发了人们对开发能够检测和可视化 DNA 甲基化的方法的极大兴趣。例如,与甲基-CpG 结合域 (MBD) 缀合的荧光蛋白 (FP) 已被用于活细胞成像的 DNA 甲基化。然而,基于 FP 的方法显示了 DNA 结合和未结合状态的荧光信号,因此难以区分这些状态。合成分子/蛋白质杂合体探针可以提供一种替代方法来克服这种限制。在本文中,我们讨论了我们最近开发的用于活细胞成像的 DNA 甲基化的合成分子/蛋白质杂合体探针,该探针仅在与甲基化 DNA 结合后才表现出荧光增强。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验