Ligand-Based Competition Binding by Real-Time 19F NMR in Human Cells

被引:2
|
作者
Luchinat, Enrico [1 ,2 ]
Barbieri, Letizia [2 ]
Davis, Ben [3 ]
Brough, Paul A. [3 ]
Pennestri, Matteo [4 ]
Banci, Lucia [2 ,5 ,6 ]
机构
[1] Univ Bologna, Dipartimento Sci & Tecnol Agroalimentari, Alma Mater Studiorum, I-47521 Cesena, Italy
[2] Consorzio Interuniv Risonanze Magnet Met Prot CIRM, I-50019 Sesto Fiorentino, Italy
[3] Vernalis Res, Cambridge CB21 6GB, England
[4] Bruker UK Ltd, Pharmaceut Business Unit, Coventry CV4 9GH, England
[5] Univ Firenze, Ctr Risonanze Magnet CERM, I-50019 Sesto Fiorentino, Italy
[6] Univ Firenze, Dipartimento Chim, I-50019 Sesto Fiorentino, Italy
基金
欧盟地平线“2020”;
关键词
LIVING CELLS; MEMBRANE-PROTEINS; IN-VITRO; INHIBITORS; CHAPERONE; SPECTROSCOPY; FLUORINE; KINETICS; SYSTEM;
D O I
10.1021/acs.jmedchem.3c01600
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The development of more effective drugs requires knowledge of their bioavailability and binding efficacy directly in the native cellular environment. In-cell nuclear magnetic resonance (NMR) spectroscopy is a powerful tool for investigating ligand-target interactions directly in living cells. However, the target molecule may be NMR-invisible due to interactions with cellular components, while observing the ligand by H-1 NMR is impractical due to the cellular background. Such limitations can be overcome by observing fluorinated ligands by F-19 in-cell NMR as they bind to the intracellular target. Here we report a novel approach based on real-time in-cell F-19 NMR that allows measuring ligand binding affinities in human cells by competition binding, using a fluorinated compound as a reference. The binding of a set of compounds toward Hsp90 alpha was investigated. In principle, this approach could be applied to other pharmacologically relevant targets, thus aiding the design of more effective compounds in the early stages of drug development.
引用
收藏
页码:1115 / 1126
页数:12
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