关于探针调制测定的 POLARISED 视图和 FRETting:从高通量筛选中学习

IF 2.7 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS SLAS Discovery Pub Date : 2024-04-18 DOI:10.1016/j.slasd.2024.100156
Alice Lanne , Catherine Bardelle , Gareth Davies , Antonia Turberville , Hannah Semple , Rachel Moore , Geoffrey A. Holdgate
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引用次数: 0

摘要

荧光探针调制测定是一种广泛使用的方法,用于监测荧光标记工具配体被测试化合物置换或稳定的情况。这些检测方法可对探针与受体的结合进行光学读数,并可用于检测与标记配体直接或间接竞争的化合物。通常采用的探针既可用于正交位点,也可用于异位位点。该方法还可用于鉴定可稳定三元复合物的测试化合物,为发现新型分子胶提供了机会。由于使用了链霉亲和素标记的铽作为供体,并可获得一系列不同的受体荧光团,这些基于荧光的检测方法在高通量筛选中的应用变得更加容易。2023 年期间,阿斯利康的高通量筛选小组利用这些方法进行了 8 次高通量筛选。在本手稿中,我们将介绍所使用的测定类型、测定开发和筛选的时间轴概述、应用正交伪影方法帮助寻找靶点的情况,以及从靶点率和鉴定出的 IC50 值优于 30 µM 的化合物数量来看筛选结果。此外,还将介绍在这些筛选的开发、执行和分析过程中学习到的知识。
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POLARISED views and FRETting about probe modulation assays: Learning from High Throughput Screening

Fluorescent probe modulation assays are a widely used approach to monitor displacement or stabilisation of fluorescently labelled tool ligands by test compounds. These assays allow an optical read-out of probe-receptor binding and can be used to detect compounds that compete with the labelled ligand, either directly or indirectly. Probes for both orthosteric and allosteric sites are often employed. The method can also be used to identify test compounds that may stabilise the ternary complex, offering an opportunity to discover novel molecular glues. The utility of these fluorescence-based assays within high-throughput screening has been facilitated by the use of streptavidin labelled terbium as a donor and access to a range of different acceptor fluorophores. During 2023, the High-throughput Screening group at AstraZeneca carried out 8 high-throughput screens using these approaches. In this manuscript we will present the types of assays used, an overview of the timelines for assay development and screening, the application of orthogonal artefact methods to aid hit finding and the results of the screens in terms of hit rate and the number of compounds identified with IC50 values of better than 30 µM. Learning across the development, execution and analysis of these screens will be presented.

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来源期刊
SLAS Discovery
SLAS Discovery Chemistry-Analytical Chemistry
CiteScore
7.00
自引率
3.20%
发文量
58
审稿时长
39 days
期刊介绍: Advancing Life Sciences R&D: SLAS Discovery reports how scientists develop and utilize novel technologies and/or approaches to provide and characterize chemical and biological tools to understand and treat human disease. SLAS Discovery is a peer-reviewed journal that publishes scientific reports that enable and improve target validation, evaluate current drug discovery technologies, provide novel research tools, and incorporate research approaches that enhance depth of knowledge and drug discovery success. SLAS Discovery emphasizes scientific and technical advances in target identification/validation (including chemical probes, RNA silencing, gene editing technologies); biomarker discovery; assay development; virtual, medium- or high-throughput screening (biochemical and biological, biophysical, phenotypic, toxicological, ADME); lead generation/optimization; chemical biology; and informatics (data analysis, image analysis, statistics, bio- and chemo-informatics). Review articles on target biology, new paradigms in drug discovery and advances in drug discovery technologies. SLAS Discovery is of particular interest to those involved in analytical chemistry, applied microbiology, automation, biochemistry, bioengineering, biomedical optics, biotechnology, bioinformatics, cell biology, DNA science and technology, genetics, information technology, medicinal chemistry, molecular biology, natural products chemistry, organic chemistry, pharmacology, spectroscopy, and toxicology. SLAS Discovery is a member of the Committee on Publication Ethics (COPE) and was published previously (1996-2016) as the Journal of Biomolecular Screening (JBS).
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