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通过荧光嵌入剂置换分析法鉴定新型DNA i-基序结合配体。

Identification of new DNA i-motif binding ligands through a fluorescent intercalator displacement assay.

作者信息

Sheng Qiran, Neaverson Joseph C, Mahmoud Tasnim, Stevenson Clare E M, Matthews Susan E, Waller Zoë A E

机构信息

School of Pharmacy, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.

Department of Biological Chemistry, John Innes Centre, Norwich Research Park, Norwich, NR4 7UH, UK.

出版信息

Org Biomol Chem. 2017 Jul 21;15(27):5669-5673. doi: 10.1039/c7ob00710h. Epub 2017 Jun 1.

Abstract

i-Motifs are quadruplex DNA structures formed from sequences rich in cytosine and held together by intercalated, hemi-protonated cytosine-cytosine base pairs. These sequences are prevalent in gene promoter regions and may play a role in gene transcription. Targeting these structures with ligands could provide a novel way to target genetic disease but there are very few ligands which have been shown to interact with i-motif DNA. Fluorescent intercalator displacement (FID) assays are a simple way to screen ligands against DNA secondary structures. Here we characterise how thiazole orange interacts with i-motif DNA and assess its ability for use in a FID assay. Additionally, we report FID-based ligand screening using thiazole orange against the i-motif forming sequence from the human telomere to reveal new i-motif binding compounds which have the potential for further development.

摘要

i-基序是由富含胞嘧啶的序列形成的四链体DNA结构,通过插入的半质子化胞嘧啶-胞嘧啶碱基对结合在一起。这些序列在基因启动子区域普遍存在,可能在基因转录中发挥作用。用配体靶向这些结构可能为治疗遗传疾病提供一种新方法,但很少有配体被证明能与i-基序DNA相互作用。荧光嵌入剂置换(FID)分析是筛选针对DNA二级结构的配体的一种简单方法。在这里,我们表征了噻唑橙与i-基序DNA的相互作用方式,并评估了其在FID分析中的应用能力。此外,我们报告了使用噻唑橙对来自人类端粒的i-基序形成序列进行基于FID的配体筛选,以揭示具有进一步开发潜力的新的i-基序结合化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064b/5708337/a6de309bf106/c7ob00710h-f1.jpg

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