• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

无标记药物筛选测定法与正交时间分辨荧光标记测定法的多重分析。

Label-free drug screening assay multiplexed with an orthogonal time-resolved fluorescence labeled assay.

机构信息

Gedeon Richter Plc, Gyömrői út 19-21, 1103, Budapest, Hungary.

Gedeon Richter Plc, Gyömrői út 19-21, 1103, Budapest, Hungary.

出版信息

Anal Biochem. 2019 Feb 1;566:126-132. doi: 10.1016/j.ab.2018.11.012. Epub 2018 Nov 16.

DOI:10.1016/j.ab.2018.11.012
PMID:30452893
Abstract

Cell-based assays against cell surface receptor targets are essential in vitro models of target-based drug discovery. At the lead generation phase large-scale functional screening assays monitoring individual cellular readouts detect interactions between the compounds and the predefined pathways but might lack sufficient sensitivity owing to the complexity of downstream signaling pathways. Cellular label-free assays offer advantages over labeled detection approaches as they reflect whole-cell responses without the prerequisite of detecting only a single cellular analyte and introducing additional genetic manipulations in favor of the chosen detection method. The combination of a label-free assay and labeled assays might integrate the advantageous characteristics of both approaches with regards to added pharmacological information and a bigger pool of chemical starting material. Here we report multiplexing of dynamic mass redistribution label-free technology with HTRF-based cAMP detection on an alpha2c adrenergic receptor expressing cell line. Besides describing the challenging assay development work associated with the set goal, a pilot screening campaign on ca. 1600 compounds is also presented. The combined assay demonstrated the ability to detect relevant activities in both readouts. Interpretation of the results as well as an outlook for further possible opportunities and applications are also discussed.

摘要

基于细胞的细胞表面受体靶标分析是基于靶标的药物发现的重要体外模型。在先导化合物生成阶段,大规模的功能筛选分析可以监测单个细胞的读出值,从而检测化合物与预先定义的途径之间的相互作用,但由于下游信号通路的复杂性,可能缺乏足够的灵敏度。细胞无标记分析相对于标记检测方法具有优势,因为它们反映了整个细胞的反应,而不需要仅检测单个细胞分析物,并且引入了额外的遗传操作,以支持所选的检测方法。无标记分析与标记分析的结合可能会整合这两种方法的优势特征,包括增加药理学信息和更大的化学起始材料库。在这里,我们报告了基于动态质量重分布的无标记技术与基于 HTRF 的 cAMP 检测在表达α2c 肾上腺素能受体的细胞系上的多重检测。除了描述与设定目标相关的具有挑战性的分析开发工作外,还介绍了大约 1600 种化合物的初步筛选活动。组合分析证明了在两种读数中都能够检测到相关的活性。还讨论了对结果的解释以及进一步可能的机会和应用的展望。

相似文献

1
Label-free drug screening assay multiplexed with an orthogonal time-resolved fluorescence labeled assay.无标记药物筛选测定法与正交时间分辨荧光标记测定法的多重分析。
Anal Biochem. 2019 Feb 1;566:126-132. doi: 10.1016/j.ab.2018.11.012. Epub 2018 Nov 16.
2
A novel cell-based duplex high-throughput screening assay combining fluorescent Ca(2+) measurement with homogeneous time-resolved fluorescence technology.一种基于细胞的新型双工高通量筛选测定法,将荧光钙(Ca2+)测量与均相时间分辨荧光技术相结合。
Anal Biochem. 2016 Aug 15;507:33-9. doi: 10.1016/j.ab.2016.05.009. Epub 2016 May 24.
3
Label-free imaging and temporal signature in phenotypic cellular assays: a new approach to high-content screening.表型细胞分析中的无标记成像和时间特征:一种高内涵筛选的新方法。
Curr Protoc Pharmacol. 2010 Sep;Chapter 9:Unit 9.13. doi: 10.1002/0471141755.ph0913s50.
4
Cell-impedance-based label-free technology for the identification of new drugs.基于细胞阻抗的无标记技术用于新药鉴定。
Expert Opin Drug Discov. 2017 Apr;12(4):335-343. doi: 10.1080/17460441.2017.1297419. Epub 2017 Mar 1.
5
Label-free screening assays: a strategy for finding better drug candidates.无标记筛选检测法:寻找更好药物候选物的策略。
Future Med Chem. 2010 Nov;2(11):1703-16. doi: 10.4155/fmc.10.246.
6
Label-free cell-based dynamic mass redistribution assays.基于无标记细胞的动态质量再分布分析
Curr Protoc Chem Biol. 2014 Mar 14;6(1):39-51. doi: 10.1002/9780470559277.ch130205.
7
Nomad Biosensors: A New Multiplexed Technology for the Screening of GPCR Ligands.游牧生物传感器:一种用于 G 蛋白偶联受体配体筛选的新型多重技术。
SLAS Technol. 2018 Jun;23(3):207-216. doi: 10.1177/2472630318754828. Epub 2018 Feb 7.
8
Enhanced selectivity screening of GPCR ligands using a label-free cell based assay technology.使用基于无标记细胞的检测技术增强GPCR配体的选择性筛选。
Comb Chem High Throughput Screen. 2009 Sep;12(8):812-23. doi: 10.2174/138620709789104861. Epub 2009 Sep 1.
9
Impact of new technologies for cellular screening along the drug value chain.细胞筛选新技术对药物价值链的影响。
Drug Discov Today. 2010 May;15(9-10):384-90. doi: 10.1016/j.drudis.2010.02.010. Epub 2010 Mar 3.
10
Comparing label-free biosensors for pharmacological screening with cell-based functional assays.将用于药理筛选的无标记生物传感器与基于细胞的功能测定进行比较。
Assay Drug Dev Technol. 2010 Apr;8(2):219-27. doi: 10.1089/adt.2009.0232.

引用本文的文献

1
Parallelized label-free monitoring of cell adhesion on extracellular matrix proteins measured by single colour reflectometry.通过单波长反射测量法对细胞在细胞外基质蛋白上的黏附进行平行的无标记监测。
Anal Bioanal Chem. 2022 Jan;414(1):575-585. doi: 10.1007/s00216-021-03522-1. Epub 2021 Jul 16.