可重用性
化学
固定化酶
色谱法
酶
药物发现
质谱法
亲和层析
组合化学
计算生物学
计算机科学
生物化学
生物
程序设计语言
软件
作者
Pamella Christina Ortega de Oliveira,Renato Lessa,Millena Santana Ceroullo,Camila Anchau Wegermann,Marcela Cristina de Moraes
标识
DOI:10.3389/frans.2022.1004113
摘要
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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