On-flow enzymatic inhibitor screening: The emerging success of liquid chromatography-based assays

Pamella Christina Ortega de Oliveira, Renato C. S. Lessa, M. S. Ceroullo, C. A. Wegermann, M. D. de Moraes
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引用次数: 2

Abstract

Enzymes are targets commonly explored in screening assays aiming to discover new leads in the drug development process. Among the diverse assay models to identify new enzymatic inhibitors, on-flow assays based on liquid chromatography (LC) can be highlighted. In these approaches, the ligand-enzyme interaction can be examined by monitoring the catalytic activity or the affinity/retention. Most applications use the biological target immobilized in solid supports resulting in the acquisition of an immobilized enzymatic reactor (IMER). Coupling IMERs to LC or mass spectrometry (MS) systems allows monitoring enzyme activity online and studying binding events between target and ligands. On-flow screening assays present many advantages for the hit-to-lead process, such as the possibility of system automation, reusability, and high stability. This review covers articles from the last decade that combine the use of varied immobilization methods on different solid supports and several equipment setups in on-flow systems, emphasizing the performance and capacity of recognizing and identifying biologically active compounds in various matrices.
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流动酶抑制剂筛选:基于液相色谱分析的新成功
酶是筛选分析中经常探索的目标,旨在发现药物开发过程中的新线索。在鉴定新的酶抑制剂的各种分析模型中,基于液相色谱(LC)的流动分析可以突出。在这些方法中,可以通过监测催化活性或亲和力/保留来检测配体与酶的相互作用。大多数应用使用固定化固体载体中的生物靶标,从而获得固定化酶反应器(IMER)。耦合IMERs到LC或质谱(MS)系统允许在线监测酶活性和研究目标和配体之间的结合事件。流动筛选分析为hit-to-lead过程提供了许多优势,例如系统自动化的可能性、可重用性和高稳定性。这篇综述涵盖了近十年来的文章,这些文章结合了在不同固体载体和流动系统中几种设备设置上的各种固定方法的使用,强调了识别和识别各种基质中生物活性化合物的性能和能力。
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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