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首页> 外文期刊>The Journal of Antibiotics: An International Journal >A label-free method for studying DNA sequence recognition of mitoxantrone based on resonance light-scattering technique
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A label-free method for studying DNA sequence recognition of mitoxantrone based on resonance light-scattering technique

机译:基于共振光散射技术研究米托蒽醌DNA序列识别的无标记方法

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摘要

A label-free method for studying DNA sequence recognition of mitoxantrone (MIT) by resonance light-scattering (RLS) technique has been developed in this contribution. Through the RLS spectra, the selective no-covalent interactions between MIT and double-stranded DNA, single-stranded DNA (ssDNA), oligonucleotides were systematically studied. The results of the experiments displayed that MIT had an obvious preference to ssDNA with the K (K RLS), 15.16 mmol mg -1 and the number of binding sites (N), 8.68 × 10 -4 mmol mg 1. Besides, it was found that MIT had a preference to sequences that were rich in guanine and cytosine bases with K RLS, 17.29 l mmol -1 and N, 1.19 × 10 -2 l mmol -1. The recognition mechanisms were well discussed and by fluorescence method and atom force microscopy, the RLS technique was confirmed to be a reliable method in this study. Compared with other methods, what the RLS strategy displayed was the direct interaction between anticancer drugs and DNA in vitro without the influence of a foreign substance. Thus, it can be a simple, fast and label-free strategy for DNA sequence recognition studies of DNA-targeted anticancer drugs.
机译:为此,开发了一种无标记方法,用于通过共振光散射(RLS)技术研究米托蒽醌(MIT)的DNA序列识别。通过RLS光谱,系统地研究了MIT与双链DNA,单链DNA(ssDNA)和寡核苷酸之间的选择性无共价相互作用。实验结果表明,MIT对ssDNA具有明显的偏爱,其K(K RLS)为15.16 mmol mg -1,结合位点数(N)为8.68×10 -4 mmol mg 1。发现MIT优先选择富含鸟嘌呤和胞嘧啶碱基且K RLS为17.29 l mmol -1和N为1.19×10 -2 l mmol -1的序列。对识别机理进行了很好的讨论,并通过荧光方法和原子力显微镜,RLS技术被认为是一种可靠的方法。与其他方法相比,RLS策略显示的是体外抗癌药物与DNA之间的直接相互作用而不受外来物质的影响。因此,对于靶向DNA的抗癌药物的DNA序列识别研究而言,这可能是一种简单,快速且无标签的策略。

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