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对阳离子和多核苷酸的直接观察解释了聚离子在带相同电荷表面的吸附现象。

Direct observation of cations and polynucleotides explains polyion adsorption to like-charged surfaces.

作者信息

Libera Joseph A, Cheng Hao, Olvera de la Cruz Monica, Bedzyk Michael J

机构信息

Department of Materials Science and Engineering and The Nanoscale Science and Engineering Center, Northwestern University, Evanston, Illinois 60208, USA.

出版信息

J Phys Chem B. 2005 Dec 8;109(48):23001-7. doi: 10.1021/jp0534941.

Abstract

We show an experimental approach for directly observing the condensation of polynucleotides and their electrolyte counterions at a liquid/solid interface. X-ray standing waves (XSW) generated by Bragg diffraction from a d = 20 nm Si/Mo multilayer substrate are used to measure the distinct distribution profiles of the polyanions and simple cations along the surface normal direction with subnanometer resolution. The 1D spatial sensitivity of this approach is enhanced by observing the XSW induced fluorescence modulations over multiple orders of Bragg peaks. We study the interesting divalent cation driven adsorption of anionic polynucleotides to anionic surfaces by exposing a hydroxyl-terminated silica surface to an aqueous solution with ZnCl2 and mercurated poly-uridylic acid (a synthetic RNA molecule). The in situ long-period XSW measurements are used to follow the evolution of both the Zn and Hg distribution profiles during the adsorption process. The conditions and physical mechanisms that govern the observed divalent cation adsorption and subsequent polynucleotide adsorption to an anionic surface are explained by a thermodynamic model that incorporates nonlinear electrostatic effects.

摘要

我们展示了一种直接观察多核苷酸及其电解质抗衡离子在液/固界面处凝聚的实验方法。由d = 20 nm的Si/Mo多层衬底的布拉格衍射产生的X射线驻波(XSW)用于以亚纳米分辨率测量聚阴离子和简单阳离子沿表面法线方向的不同分布轮廓。通过观察多个布拉格峰阶次上的XSW诱导荧光调制,增强了该方法的一维空间灵敏度。我们通过将羟基封端的二氧化硅表面暴露于含有ZnCl2和汞化聚尿苷酸(一种合成RNA分子)的水溶液中,研究了有趣的二价阳离子驱动的阴离子多核苷酸对阴离子表面的吸附。原位长周期XSW测量用于跟踪吸附过程中Zn和Hg分布轮廓的演变。一个纳入非线性静电效应的热力学模型解释了控制观察到的二价阳离子吸附以及随后多核苷酸吸附到阴离子表面的条件和物理机制。

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