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Excessive Counterion Condensation on Immobilized ssDNA in Solutions of High Ionic Strength

机译:高离子强度溶液中固定化ssDNA的过度抗衡离子缩合

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摘要

We present experiments on the bias-induced release of immobilized, single-stranded (ss) 24-mer oligonucleotides from Au-surfaces into electrolyte solutions of varying ionic strength. Desorption is evidenced by fluorescence measurements of dye-labeled ssDNA. Electrostatic interactions between adsorbed ssDNA and the Au-surface are investigated with respect to 1), a variation of the bias potential applied to the Au-electrode; and 2), the screening effect of the electrolyte solution. For the latter, the concentration of monovalent salt in solution is varied from 3 to 1600 mM. We find that the strength of electric interaction is predominantly determined by the effective charge of the ssDNA itself and that the release of DNA mainly occurs before the electrochemical double layer has been established at the electrolyte/Au interface. In agreement with Manning's condensation theory, the measured desorption efficiency (ηrel) stays constant over a wide range of salt concentrations; however, as the Debye length is reduced below a value comparable to the axial charge spacing of the DNA, ηrel decreases substantially. We assign this effect to excessive counterion condensation on the DNA in solutions of high ionic strength. In addition, the relative translational diffusion coefficient of ssDNA in solution is evaluated for different salt concentrations.
机译:我们目前对固定诱导的单链(ss)24-mer寡核苷酸从Au表面偏向释放到不同离子强度的电解质溶液中的诱导诱导释放的实验。脱附由染料标记的ssDNA的荧光测量证明。关于1)研究吸附的ssDNA与Au表面之间的静电相互作用,1)施加到Au电极上的偏置电势的变化; 2)电解液的屏蔽效果。对于后者,溶液中一价盐的浓度为3至1600 mM。我们发现电相互作用的强度主要取决于ssDNA本身的有效电荷,并且DNA的释放主要发生在电解质/ Au界面上已建立电化学双层之前。与曼宁的缩合理论相一致,测得的解吸效率(ηrel)在很宽的盐浓度范围内保持恒定。然而,由于德拜长度减小到低于可与DNA的轴向电荷间隔相当的值,ηrel显着减小。我们将此效应归因于高离子强度溶液中DNA上过度的抗衡离子缩合。此外,针对不同的盐浓度评估了ssDNA在溶液中的相对翻译扩散系数。

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