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Mass spectrometry-based Cellular Thermal Shift Assay (CETSA (R)) for target deconvolution in phenotypic drug discovery

机译:基于质谱基的细胞热移测定(CETSA(R))在表型药物发现中的靶去卷积

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The recent renewed interest in phenotypic drug discovery has concomitantly put a focus on target deconvolution in order to achieve drug-target identification. Even though there are prescribed therapies whose mode of action is not fully understood, knowledge of the primary target will inevitably facilitate the discovery and translation of efficacy from bench to bedside. Elucidating targets and subsequent pathways engaged will also facilitate safety studies and overall development of novel drug candidates. Today, there are several techniques available for identifying the primary target, many of which rely on mass spectrometry (MS) to identify compound - target protein interactions. The Cellular Thermal Shift Assay (CETSA (R)) is well suited for identifying target engagement between ligands and their protein targets. Several studies have shown that CETSA combined with MS is a powerful technique that allows unlabeled target deconvolution in complex samples such as intact cells and tissues in addition to cell lysates and other protein suspensions. The applicability of CETSA MS for target deconvolution purposes will be discussed and exemplified in this mini review.
机译:近期对表型药物发现的兴趣始终侧重于目标解卷积,以实现药物目标鉴定。尽管存在不完全理解的行动方式的规定的疗法,但主要目标的知识将不可避免地促进从长凳到床边的功效的发现和翻译。阐明的目标和随后的途径均可促进新型药物候选人的安全性研究和整体发展。如今,存在几种可用于鉴定主要目标的技术,其中许多依赖于质谱(MS)以鉴定复合靶蛋白相互作用。细胞热移测定(CETSA(R))非常适合于鉴定配体和其蛋白质靶标之间的靶接合。几项研究表明,CETSA结合MS是一种强大的技术,除了细胞裂解物和其他蛋白质悬浮液之外,还允许复杂的样品中的复杂样品中的未标记的靶去卷积。将讨论CESA MS对目标去卷积目的的适用性,并在本次审议中讨论和举例说明。

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