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首页> 外文期刊>ACS Omega >Label-Free Detecting of the Compaction and Decompaction of ctDNA Molecules Induced by Surfactants with SERS Based on a nanoPAA-ZnCl2-AuLs Solid Substrate
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Label-Free Detecting of the Compaction and Decompaction of ctDNA Molecules Induced by Surfactants with SERS Based on a nanoPAA-ZnCl2-AuLs Solid Substrate

机译:基于nanoPAA-ZnCl2-AuLs固体底物的无标记检测表面活性剂与SERS诱导的ctDNA分子的压缩和解压缩

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DNA molecular compaction/decompaction is of great significance for the exploration of basic life processes, the research of biomedical and genetic engineering, and so forth. However, the detailed mechanism of DNA compaction/decompaction caused by surfactants remains an open and challenging problem that has not been fully solved so far. In this paper, a sort of novel solid substrate, nanoPAA-ZnCl2-AuLs, with good stability and high sensitivity, was prepared by a self-assembly method. Based on this substrate, the surface-enhanced Raman scattering (SERS) technology was employed to investigate characteristics of interactions between DNA molecules and surfactants at a single molecular level. SERS spectra of calf thymus DNA (ctDNA), cetyl trimethyl ammonium bromide (CTAB), and sodium dodecyl sulfate (SDS) with a concentration as low as 10–9 M, and SERS spectra of ctDNA–CTAB and ctDNA–CTAB–SDS composites were collected, respectively. The interactions between ctDNA and surfactants were analyzed by changes in SERS spectra, for example, disappearances and appearances of SERS bands and relative changes of peak intensity, in which CTAB resulted in the compaction of the DNA molecule while SDS induced the decompaction of the ctDNA–CTAB complex. Moreover, UV–visible spectrophotometry was employed to demonstrate the compaction/decompaction of ctDNA molecules caused by surfactants. The local binding modes of ctDNA molecules and surfactant molecules were expounded. This work will be helpful for understanding biological processes such as DNA compaction and recombination within nucleus or/and cells and for the development of gene therapy technologies.
机译:DNA分子的压缩/解压缩对于基本生命过程的探索,生物医学和基因工程的研究等具有重要意义。但是,由表面活性剂引起的DNA压缩/分解的详细机理仍然是一个开放且具有挑战性的问题,到目前为止尚未完全解决。本文通过自组装法制备了一种稳定性好,灵敏度高的新型固体底物nanoPAA-ZnCl2-AuLs。基于这种基质,采用了表面增强拉曼散射(SERS)技术来研究单分子水平上DNA分子与表面活性剂之间相互作用的特性。浓度低至10–9 M的小牛胸腺DNA(ctDNA),十六烷基三甲基溴化铵(CTAB)和十二烷基硫酸钠(SDS)的SERS光谱,以及ctDNA–CTAB和ctDNA–CTAB–SDS复合材料的SERS光谱分别收集。 ctDNA与表面活性剂之间的相互作用通过SERS光谱的变化进行了分析,例如,SERS谱带的消失和出现以及峰强度的相对变化,其中CTAB导致DNA分子致密,而SDS导致ctDNA的分解。 CTAB复合物。此外,采用紫外可见分光光度法来证明由表面活性剂引起的ctDNA分子的压缩/分解。阐述了ctDNA分子与表面活性剂分子的局部结合方式。这项工作将有助于理解生物学过程,例如细胞核或细胞和/或细胞内的DNA压缩和重组,以及基因治疗技术的发展。

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