Faculty of Pharmaceutical Sciences, Teikyo University, Itabashi City, Tokyo, Japan.
Methods Mol Biol. 2020;2132:29-37. doi: 10.1007/978-1-0716-0430-4_4.
The greatest advantage of frontal affinity chromatography (FAC) is that the analyte concentration does not need to be taken into consideration, and this renders FAC an extremely favorable analytical tool for weak interactions. In this short review, we propose a straightforward explanation of the underlying mechanism. When FAC is performed using analyte solutions at relatively high concentrations, concentration-dependent retardation is observed due to competition among analyte molecules, and the elution volume changes depending on the degree of saturation of the immobilized ligand.However, when the analyte concentration is very low, no competition occurs among the analytes, and the elution volume reaches a constant value, which reflects the proportion of bound state to free state of a single analyte molecule. Therefore, the binding strength can be determined using a minimum analyte concentration.
正面亲和色谱(FAC)的最大优势在于无需考虑分析物浓度,这使得 FAC 成为弱相互作用的极其有利的分析工具。在这篇简短的综述中,我们提出了一个对其基本机制的简单解释。当使用相对较高浓度的分析物溶液进行 FAC 时,由于分析物分子之间的竞争,会观察到浓度依赖性的延迟,并且洗脱体积会根据固定化配体的饱和度而变化。然而,当分析物浓度非常低时,分析物之间不会发生竞争,洗脱体积达到一个恒定值,反映单个分析物分子的结合态与游离态的比例。因此,可以使用最小分析物浓度来确定结合强度。