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DNA-EB in agarose gel assay: a simple methodology in the search for DNA-binders in crude extracts from actinomycetes

机译:琼脂糖凝胶测定中的DNA-EB:一种简单的方法,用于寻找放线菌粗提物中的DNA结合剂

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摘要

DNA is known as a potential therapeutic target for the development of anticancer and antibiotic agents because any damage on its structure may lead to cell death. Discovery of ligand molecules through interactions with DNA is a key step in the development of new therapies. Here, a methodology was proposed to detect DNA-binders in a screening process with crude extracts produced by actinomycetes. This assay consists of a DNA-EB (ethidium bromide) complex added previously, into a simple agarose gel, where EB may be replaced by other metabolites, present in the sample added before over the gel. The free dye is washed and, consequently, the fluorescence intensity decreases. The assay results were recorded by photographs and the fluorescence intensity was transposed in pixel values using Image J software, allowing statistical analyses. The developed assay can also be applied directly onto TLC plates. Sixteen crude extracts produced by actinomycetes were screened using the developed assay, in which four crude extracts showed a significant fluorescence decrease. Dereplication studies with mass spectra data allowed the identification of anthracyclines such as Ditrisarubicin F and G in one of the selected extracts. The methodology developed here is a promising approach for drug discovery because it may lead to the detection of DNA-binding compounds in a simple, low cost way and without isolation and/or purification processes.
机译:DNA被公认为是抗癌和抗生素治疗的潜在治疗靶标,因为其结构上的任何破坏都可能导致细胞死亡。通过与DNA的相互作用发现配体分子是开发新疗法的关键步骤。在此,提出了一种方法,用于在筛选过程中用放线菌产生的粗提物检测DNA结合物。该测定法由预先添加到简单琼脂糖凝胶中的DNA-EB(溴化乙锭)复合物组成,其中EB可能被存在于凝胶上的样品中的其他代谢物所代替。洗涤游离染料,结果荧光强度降低。通过照片记录测定结果,并使用Image J软件将荧光强度转换为像素值,从而进行统计分析。开发的检测方法也可以直接应用于TLC板上。使用开发的分析方法筛选了放线菌产生的16种粗提物,其中4种粗提物显示出明显的荧光下降。利用质谱数据进行重复数据删除研究,可以鉴定出所选提取物中的一种蒽环类药物,如Ditrisarubicin F和G。此处开发的方法是一种有前途的药物发现方法,因为它可能导致以简单,低成本的方式检测DNA结合化合物,而无需分离和/或纯化过程。

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