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一种用于自动生物发光激酶选择性分析的灵活工作流程。

A Flexible Workflow for Automated Bioluminescent Kinase Selectivity Profiling.

机构信息

1 Promega Corporation, R&D Department, Madison, WI, USA.

3 Exact Sciences Corporation, Madison, WI, USA.

出版信息

SLAS Technol. 2017 Apr;22(2):153-162. doi: 10.1177/2211068216677248. Epub 2016 Nov 15.

DOI:10.1177/2211068216677248
PMID:28095176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5418932/
Abstract

Kinase profiling during drug discovery is a necessary process to confirm inhibitor selectivity and assess off-target activities. However, cost and logistical limitations prevent profiling activities from being performed in-house. We describe the development of an automated and flexible kinase profiling workflow that combines ready-to-use kinase enzymes and substrates in convenient eight-tube strips, a bench-top liquid handling device, ADP-Glo Kinase Assay (Promega, Madison, WI) technology to quantify enzyme activity, and a multimode detection instrument. Automated methods were developed for kinase reactions and quantification reactions to be assembled on a Gilson (Middleton, WI) PIPETMAX, following standardized plate layouts for single- and multidose compound profiling. Pipetting protocols were customized at runtime based on user-provided information, including compound number, increment for compound titrations, and number of kinase families to use. After the automated liquid handling procedures, a GloMax Discover (Promega) microplate reader preloaded with SMART protocols was used for luminescence detection and automatic data analysis. The functionality of the automated workflow was evaluated with several compound-kinase combinations in single-dose or dose-response profiling formats. Known target-specific inhibitions were confirmed. Novel small molecule-kinase interactions, including off-target inhibitions, were identified and confirmed in secondary studies. By adopting this streamlined profiling process, researchers can quickly and efficiently profile compounds of interest on site.

摘要

在药物发现过程中进行激酶谱分析是确认抑制剂选择性和评估非靶标活性的必要过程。然而,成本和物流限制使得内部无法进行分析。我们描述了一种自动化和灵活的激酶谱分析工作流程的开发,该工作流程将即用型激酶酶和底物结合在方便的 8 管条中,使用台式液体处理设备,ADP-Glo 激酶测定法(Promega,Madison,WI)技术来定量酶活性,以及多模式检测仪器。为了在吉尔森(Middleton,WI)PIPETMAX 上组装激酶反应和定量反应,开发了自动化方法,遵循用于单剂量和多剂量化合物分析的标准化板布局。基于用户提供的信息,包括化合物编号、化合物滴定的增量以及要使用的激酶家族数量,在运行时自定义移液协议。在自动化液体处理程序之后,使用预加载 SMART 协议的 GloMax Discover(Promega)微孔板读取器进行发光检测和自动数据分析。通过在单剂量或剂量反应分析格式中使用几种化合物-激酶组合来评估自动化工作流程的功能。确认了已知的靶标特异性抑制作用。在后续研究中,确定并确认了新型小分子-激酶相互作用,包括非靶标抑制作用。通过采用这种简化的分析流程,研究人员可以快速有效地在现场分析感兴趣的化合物。

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