Affinity Chromatography: A Powerful Tool in Drug Discovery for Investigating Ligand/membrane Protein Interactions

Lucile Lecas, V. Dugas, C. Demesmay
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引用次数: 5

Abstract

ABSTRACT Affinity chromatography is an often overlooked chromatographic technique regarding receptor/ligand studies. Indeed, biologists have a tendency to focus on more recent biophysical techniques such as NMR or surface plasmon resonance methods, among others. However, in order to face challenges related to the use of membrane proteins in drug discovery, alternative and/or complementary methods are welcome. In this frame, chromatographic methods, through the affinity mode, bring new perspectives due to their relative simplicity and the great diversity of information that they can provide. Affinity chromatography methods rely on the immobilization of targets on the stationary phase and this step is crucial when dealing with membrane proteins. Different immobilization strategies with their own specificities (surface density, nonspecific interaction, complex surface chemistry of the taking or release step) were developed allowing to encompass a wide range of applications: from ligand-ranking (synthetic compounds of medium to high affinity) to fragment screening (small compounds of weak affinity), adsorption, distribution, metabolism, and excretion studies or identification of active components from natural extracts.
亲和层析:研究配体/膜蛋白相互作用的药物发现的有力工具
亲和色谱是一种经常被忽视的用于受体/配体研究的色谱技术。事实上,生物学家倾向于关注最近的生物物理技术,如核磁共振或表面等离子体共振方法等。然而,为了应对与膜蛋白在药物发现中的应用相关的挑战,替代和/或补充方法是受欢迎的。在这个框架下,通过亲和模式的色谱方法由于其相对简单和可以提供的信息的多样性而带来了新的视角。亲和层析方法依赖于固定相上目标的固定化,这一步在处理膜蛋白时至关重要。不同的固定策略具有各自的特异性(表面密度,非特异性相互作用,摄取或释放步骤的复杂表面化学),允许包含广泛的应用:从配体排序(中高亲和力的合成化合物)到片段筛选(弱亲和力的小化合物),吸附,分布,代谢和排泄研究或天然提取物活性成分的鉴定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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