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Discovery of Small-Molecule Stabilizers of 14-3-3 Protein-Protein Interactions via Dynamic Combinatorial Chemistry
被引:20
|作者:
Hartman, Alwin M.
[1
,2
,3
]
Elgaher, Walid A. M.
[2
]
Hertrich, Nathalie
[2
]
Andrei, Sebastian A.
[4
,5
]
Ottmann, Christian
[4
,5
,6
]
Hirsch, Anna K. H.
[1
,2
,3
]
机构:
[1] Univ Groningen, Stratingh Inst Chem, NL-9747 AG Groningen, Netherlands
[2] Helmholtz Inst Pharmaceut Res Saarland HIPS, Helmholtz Ctr Infect Res HZI, Dept Drug Design & Optimizat, D-66123 Saarbrucken, Germany
[3] Saarland Univ, Dept Pharm, D-66123 Saarbrucken, Germany
[4] Eindhoven Univ Technol, Dept Biomed Engn, Lab Chem Biol, NL-5600 MB Eindhoven, Netherlands
[5] Eindhoven Univ Technol, ICMS, NL-5600 MB Eindhoven, Netherlands
[6] Univ Duisburg Essen, Dept Chem, D-47057 Essen, Germany
来源:
基金:
欧洲研究理事会;
关键词:
Protein-protein interactions;
DCC;
hit-identification strategy;
small-molecule stabilizers;
INHIBITORS;
IDENTIFICATION;
BINDING;
MODULATORS;
D O I:
10.1021/acsmedchemlett.9b00541
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Protein-protein interactions (PPIs) play an important role in numerous biological processes such as cell-cycle regulation and multiple diseases. The family of 14-3-3 proteins is an attractive target as they serve as binding partner to various proteins and are therefore capable of regulating their biological activities. Discovering small-molecule modulators, in particular stabilizers, of such complexes via traditional screening approaches is a challenging task. Herein, we pioneered the first application of dynamic combinatorial chemistry (DCC) to a PPI target, to find modulators of 14-3-3 proteins. Evaluation of the amplified hits from the DCC experiments for their binding affinity via surface plasmon resonance (SPR), revealed that the low-micromolar (K-D 15-16 mu M) acylhydrazones are 14-3-3/synaptopodin PPI stabilizers. Thus, DCC appears to be ideally suited for the discovery of not only modulators but even the more elusive stabilizers of notoriously challenging PPIs.
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页码:1041 / 1046
页数:6
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