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Biophysical study of DNA at single molecule level using solid-state nanopores

机译:使用固态纳米孔在单分子水平上对DNa进行生物物理研究

摘要

Since the discovery of deoxyribonucleic acid (DNA) over 140 years ago, this biomolecule still remains one the most studied macromolecules in nature. The modifications and interactions associated with this duplex biopolymer have been shown to play fundamental roles in cellular machinery. udThis research project exploited sets of single-molecule detection techniques in parallel with conventional molecular biology methodologies to study i) chemical modification (methylation) of the DNA and its functional role and ii) electrostatic interaction between two homologous DNA duplexes. In this project solid-state nanopores were utilised as a novel approach to probe structural and conformational changes of linear and circular DNA.udTo begin with, the effect of DNA methylation level in breast cancer cell-lines was investigated. Using solid-state nanopore sensors and a methyl specific antibody (5’-mc), the methylated and unmethylated regions of FOXA1 (a gene associated with breast cancer development) promoter were differentiated. Simultaneously, the methylation level of this gene was evaluated in various breast cancer cell-lines and confirmed the impact of DNA methylation in gene silencing. In addition, using atomic force microscopy analysis, the binding affinity of the antibody to the methylated DNA was determinedudFurthermore, by employing the same methodologies, the presence of an electrostatic recognition step in homologous segments of a bacteria plasmid within the framework of Kornyshev-Leikin theory was investigated. However to this end, the verification of this model was inconclusive. Nevertheless it was serendipitously found that the plasmid with homologous regions was dimerised and then formed a single loop. This finding would be the motivation behind further experiments to gain a better understanding of the possible sequence dependence of the DNA topology and configuration during cloning and amplification procedures. Furthermore, using a combination of various techniques, the biophysical properties of the monomeric and dimeric plasmids were characterised.udOverall, the combined findings of the mentioned projects provided remarkable insights on the molecular biophysics of DNA-DNA and DNA-protein interactions within the framework of the central dogma of molecular biology.
机译:自140年前发现脱氧核糖核酸(DNA)以来,这种生物分子仍然是自然界中研究最多的大分子之一。已经显示出与这种双工生物聚合物相关的修饰和相互作用在细胞机械中起着基本作用。 ud此研究项目与常规分子生物学方法相结合,利用了一系列单分子检测技术来研究i)DNA的化学修饰(甲基化)及其功能作用,以及ii)两个同源DNA双链体之间的静电相互作用。在该项目中,固态纳米孔被用作探测线性和环状DNA结构和构象变化的新方法。 ud首先,研究了DNA甲基化水平对乳腺癌细胞系的影响。使用固态纳米孔传感器和甲基特异性抗体(5'-mc),区分了FOXA1(与乳腺癌发展相关的基因)启动子的甲基化和非甲基化区域。同时,在各种乳腺癌细胞系中评估了该基因的甲基化水平,并证实了DNA甲基化对基因沉默的影响。此外,使用原子力显微镜分析,还确定了抗体与甲基化DNA的结合亲和力 ud此外,采用相同的方法,在科尔尼雪夫(Kornyshev-)框架内细菌质粒的同源片段中存在静电识别步骤。研究了雷金理论。但是,为此目的,该模型的验证尚无定论。然而,偶然发现具有同源区域的质粒被二聚化,然后形成单个环。这一发现将成为进一步实验的动机,以便在克隆和扩增过程中更好地了解DNA拓扑结构和构型的可能序列依赖性。此外,使用各种技术的组合,对单体和二聚体质粒的生物物理特性进行了表征。 ud总体而言,上述项目的综合发现为框架内DNA-DNA和DNA-蛋白质相互作用的分子生物物理学提供了深刻的见解。分子生物学的中心教条。

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    Bahrami Azadeh;

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  • 年度 2014
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