DNA binding to small anionic ligands: the case of Orange G dye

IF 2.2 4区 生物学 Q3 BIOPHYSICS
Rayane M. de Oliveira, Arthur G. S. de Rezende, Daniel F. Campos, Neemias de A. Ribeiro, Márcio S. Rocha
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引用次数: 0

Abstract

Here we advance in the understanding of nucleic acids interactions with small anionic ligands by characterizing the binding of the Orange G (OG) dye to double-stranded DNA via single molecule force spectroscopy. While there is no detectable interaction at low ionic strengths, we found that for [\(\hbox {Na}^+\)] = 150 mM OG was able to interact with the double-helix via groove binding in a non-cooperative way, with a relatively high equilibrium association constant (\(\sim\) \(10^5\) \(\hbox {M}^{-1}\)) that is compatible to other classic DNA small ligands. Furthermore, experiments performed with a fixed OG concentration at various ionic strengths clearly show that the binding can be turned “on / off” by regulating the concentration of available counterions, a result that can guide the development of new synthetic ligands and shows how to modulate their interactions with nucleic acids. The present work therefore advances in evaluating the fundamental role of the ionic strength on the DNA interactions with small anionic ligands.

Abstract Image

DNA与小阴离子配体的结合:橙色G染料的例子。
在这里,我们通过单分子力谱表征橙色G (OG)染料与双链DNA的结合,进一步了解了核酸与小阴离子配体的相互作用。虽然在低离子强度下没有检测到相互作用,但我们发现,对于[Na +] = 150 mM, OG能够以非合作方式通过槽结合与双螺旋相互作用,具有相对较高的平衡结合常数(~ 10.5 M - 1),与其他经典DNA小配体兼容。此外,在不同离子强度的固定OG浓度下进行的实验清楚地表明,可以通过调节可用反离子的浓度来“打开/关闭”这种结合,这一结果可以指导新合成配体的开发,并展示如何调节它们与核酸的相互作用。因此,目前的工作在评估离子强度在DNA与小阴离子配体相互作用中的基本作用方面取得了进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Biophysics Journal
European Biophysics Journal 生物-生物物理
CiteScore
4.30
自引率
0.00%
发文量
43
审稿时长
6-12 weeks
期刊介绍: The journal publishes papers in the field of biophysics, which is defined as the study of biological phenomena by using physical methods and concepts. Original papers, reviews and Biophysics letters are published. The primary goal of this journal is to advance the understanding of biological structure and function by application of the principles of physical science, and by presenting the work in a biophysical context. Papers employing a distinctively biophysical approach at all levels of biological organisation will be considered, as will both experimental and theoretical studies. The criteria for acceptance are scientific content, originality and relevance to biological systems of current interest and importance. Principal areas of interest include: - Structure and dynamics of biological macromolecules - Membrane biophysics and ion channels - Cell biophysics and organisation - Macromolecular assemblies - Biophysical methods and instrumentation - Advanced microscopics - System dynamics.
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