强度消退MALDI-TOF-MS:新的配体结合筛选和药物发现

Óscar Yanes , Josep Villanueva , Enrique Querol , Francesc X. Aviles
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引用次数: 12

摘要

配体发现技术在很大程度上依赖于对显示与靶标亲和力的分子的初步筛选,以及识别这些分子的方法。基质辅助激光解吸电离(MALDI)飞行时间(TOF)质谱(MS)作为一种适合于配体鉴定的分析技术,因其高灵敏度和鉴别能力、快速分析和易于自动化而越来越受到人们的关注。现在有一系列相关的药物发现策略,包括一种新的基于质谱的方法,用于筛选大分子靶标(蛋白酶)和肽或有机配体(蛋白酶抑制剂)之间的非共价相互作用,称为强度消退(IF) MALDI-TOF-MS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intensity-fading MALDI-TOF-MS: novel screening for ligand binding and drug discovery

Ligand discovery technologies largely rely on a primary screening for molecules showing affinity to a target, coupled with an approach to identify these molecules. Matrix-assisted laser desorption ionization (MALDI) time-of-flight (TOF) mass spectrometry (MS) is attracting increasing attention as a suitable analytical technique for ligand identification owing to its high sensitivity and capacity for discrimination, its fast analysis and its ease of automation. There is now a range of related strategies for drug discovery, including a novel MS-based methodology to screen noncovalent interactions between macromolecular targets (proteases) and peptide or organic ligands (protease inhibitors) called intensity-fading (IF) MALDI-TOF-MS.

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