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线性和过载条件下线性质粒DNA与阴离子交换支持物相互作用的热力学研究

Thermodynamic study of the interaction between linear plasmid DNA and an anion exchange support under linear and overloaded conditions.

作者信息

Aguilar P A, Twarda A, Sousa F, Dias-Cabral A C

机构信息

CICS-UBI - Health Sciences Research Centre, University of Beira Interior, 6200-506 Covilhã, Portugal; Department of Chemistry, University of Beira Interior, 6200-001 Covilhã, Portugal.

CICS-UBI - Health Sciences Research Centre, University of Beira Interior, 6200-506 Covilhã, Portugal; Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 30-387 Cracow, Poland.

出版信息

J Chromatogr A. 2014 Dec 12;1372C:166-173. doi: 10.1016/j.chroma.2014.11.002. Epub 2014 Nov 7.

Abstract

Anion-exchange chromatography has been successfully used in plasmid DNA (pDNA) purification. However, pDNA adsorption mechanism using this method is still not completely understood, and the prediction of the separation behavior is generally unreliable. Flow microcalorimetry (FMC) has proven its ability to provide an improved understanding of the driving forces and mechanisms involved in the adsorption process of biomolecules onto several chromatographic systems. Thus, using FMC, this study aims to understand the adsorption mechanism of linear pDNA (pVAX1-LacZ) onto the anion-exchange support Fast Flow (FF) Q-Sepharose. Static binding capacity studies have shown that the mechanism of pDNA adsorption onto Q-Sepharose follows a Langmuir isotherm. FMC experiments resulted in thermograms that comprised endothermic and exothermic heats. Endothermic heat major contributor was suggested to be the desolvation process. Exothermic heats were related to the interaction between pDNA and Q-Sepharose primary and secondary adsorption. Furthermore, FMC revealed that the overall adsorption process is exothermic, as expected for an anion-exchange interaction. Nevertheless, there are evidences of the presence of nonspecific effects, such as reorientation and electrostatic repulsive forces.

摘要

阴离子交换色谱已成功应用于质粒DNA(pDNA)的纯化。然而,使用该方法的pDNA吸附机制仍未完全了解,并且分离行为的预测通常不可靠。流动微量热法(FMC)已证明其能够更好地理解生物分子在几种色谱系统上吸附过程中涉及的驱动力和机制。因此,本研究旨在利用FMC了解线性pDNA(pVAX1-LacZ)在阴离子交换载体快速流动(FF)Q-琼脂糖上的吸附机制。静态结合容量研究表明,pDNA在Q-琼脂糖上的吸附机制遵循朗缪尔等温线。FMC实验得到的热谱图包含吸热和放热。吸热的主要贡献者被认为是去溶剂化过程。放热与pDNA和Q-琼脂糖的一级和二级吸附之间的相互作用有关。此外,FMC表明,总体吸附过程是放热的,这与阴离子交换相互作用的预期一致。然而,有证据表明存在非特异性效应,如重新定向和静电排斥力。

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