通过相对迁移率偏移部分填充亲和性毛细管电泳测定金属-生物分子相互作用

IF 3.6 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Analyst Pub Date : 2024-11-17 DOI:10.1039/d4an01176g
Tao Huang, Jinxiang Xu, Chunsu Liang, Liyu Gong, Xiaomei Ling
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引用次数: 0

摘要

金属离子及其与生物大分子的相互作用对人类健康起着重要作用。然而,常用于 HPCE 的光学检测器在没有紫外线吸收的情况下无法直接检测金属离子。为了弥补现有 HPCE 检测器的不足,一种新型的通用 HPCE 检测系统--界面诱导电流检测器(IIRRD)应运而生。与此同时,大多数关于金属-生物大分子相互作用的研究仅关注于生物大分子的检测和分析,普遍存在结果不准确或假阴性的问题,这一点尚待解决。在此,应用 HPCE-IICRD 首次实现了直接测量金属离子电泳参数来测定金属-生物大分子相互作用,表明可以更直接、更准确地测量相互作用强度。此外,为了定量分析金属与生物大分子的结合强度,研究人员还开发了一种改进的亲和性毛细管电泳(ACE)方法--相对迁移率偏移部分填充ACE-IICRD(rmsPF-ACE-IICRD)。研究了12种游离金属离子与3种生物大分子(包括2种血液蛋白、2种酶蛋白和2种原生DNA)的结合行为,并利用非线性色谱法(NLC)计算和评价了金属-生物大分子复合物的平衡解离常数(KD)值。实验结果与文献值基本一致。其中,重金属离子与蛋白质和酶的相互作用更强,而金属离子与原生 DNA 的结合力往往强于蛋白质和酶,这与文献结果一致。HPCE-IICRD与rmsPF-ACE的联合使用具有无需前处理、操作成本低、重复性好、操作简单、无共存物质干扰等优点,有望成为一种高效的金属离子检测方法,也将拓展IICRD的应用范围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of metal-biomolecule interactions by relative mobility shift partial filling affinity capillary electrophoresis
Metal ions and their interactions with biomolecules play an important role in human health. However, optical detectors commonly used for HPCE cannot directly detect metal ions without UV absorption. To make up the shortcomings of existing HPCE detectors, a new universal HPCE detection system called interface-induced current detector (IICRD) has been constructed previously, with no need of derivatization procedures or complex instrumental modifications. Meanwhile, most of the reported studies on metal-biomolecule interactions only focused on the detection and analysis of biomolecules, commonly causing inaccurate or false-negative results, which was yet to be resolved. Here, the application of HPCE-IICRD realized the determination of metal-biomolecule interactions by directly measuring the electrophoretic parameters of metal ions for the first time, indicating that the interaction intensity can be measured more directly and accurately. Furthermore, an improved affinity capillary electrophoresis (ACE) method called relative mobility shift partial filling ACE-IICRD (rmsPF-ACE-IICRD) was originally developed to quantitatively analyze the binding strength. Binding behaviors between twelve free metal ions and three types of biomolecules (including two blood proteins, two enzyme proteins and two native DNAs) were investigated, and the values of equilibrium dissociation constant (KD) of metal-biomolecule complexes were calculated and evaluated by nonlinear chromatography (NLC) method. The experimental results were basically consistent with the literature values. In particular, heavy metal ions showed stronger interactions with proteins and enzymes, while metal ions tended to show stronger binding with native DNAs than proteins and enzymes, which were in agreement with literature results. The combined use of HPCE-IICRD and rmsPF-ACE showed great advantages such as no need of pretreatment, low operating cost, good repeatability, simple operation and no interference of coexisting substances, which is hopeful to become an efficient metal ion detection method, also to expand the application scope of IICRD in the future.
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来源期刊
Analyst
Analyst 化学-分析化学
CiteScore
7.80
自引率
4.80%
发文量
636
审稿时长
1.9 months
期刊介绍: The home of premier fundamental discoveries, inventions and applications in the analytical and bioanalytical sciences
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