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基于纳米聚丙烯酸锌-金纳米棒固体基底的表面增强拉曼光谱法对表面活性剂诱导的ctDNA分子压缩与解压缩的无标记检测

Label-Free Detecting of the Compaction and Decompaction of ctDNA Molecules Induced by Surfactants with SERS Based on a nanoPAA-ZnCl-AuLs Solid Substrate.

作者信息

Hao Bojuan, Wang Kaige, Zhou Yukun, Sui Chaofan, Wang Lei, Bai Ren, Yang Zhaojin

机构信息

State Key Laboratory of Cultivation Base for Photoelectric Technology and Functional Materials, Laboratory of Optoelectronic Technology of Shaanxi Province, National Center for International Research of Photoelectric Technology & Nano-Functional Materials and Application, Institute of Photonics and Photon-Technology, Northwest University, Xi'an 710069, China.

Xi'an Institute of Applied Optics, Xi'an 710065, China.

出版信息

ACS Omega. 2020 Jan 7;5(2):1109-1119. doi: 10.1021/acsomega.9b03294. eCollection 2020 Jan 21.

Abstract

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-ZnCl-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 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.

摘要

DNA分子的压缩/解压缩对于探索基本生命过程、生物医学和基因工程研究等具有重要意义。然而,表面活性剂引起的DNA压缩/解压缩的详细机制仍然是一个尚未完全解决的开放性难题。本文通过自组装方法制备了一种具有良好稳定性和高灵敏度的新型固体基底nanoPAA-ZnCl-AuLs。基于该基底,采用表面增强拉曼散射(SERS)技术在单分子水平上研究DNA分子与表面活性剂之间的相互作用特性。分别收集了浓度低至10 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复合物的SERS光谱。通过SERS光谱的变化,如SERS谱带的消失和出现以及峰强度的相对变化,分析了ctDNA与表面活性剂之间的相互作用,其中CTAB导致DNA分子压缩,而SDS诱导ctDNA-CTAB复合物解压缩。此外,采用紫外可见分光光度法证明了表面活性剂引起的ctDNA分子的压缩/解压缩。阐述了ctDNA分子与表面活性剂分子的局部结合模式。这项工作将有助于理解细胞核或/和细胞内的DNA压缩和重组等生物过程以及基因治疗技术的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6fc/6977030/fed714d4ed8e/ao9b03294_0001.jpg

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