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首页> 外文期刊>ACS medicinal chemistry letters >Discovery of Small-Molecule Stabilizers of 14-3-3 Protein-Protein Interactions via Dynamic Combinatorial Chemistry
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Discovery of Small-Molecule Stabilizers of 14-3-3 Protein-Protein Interactions via Dynamic Combinatorial Chemistry

机译:通过动态组合化学发现14-3-3蛋白 - 蛋白质相互作用的小分子稳定剂

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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.
机译:蛋白质 - 蛋白质相互作用(PPI)在许多生物过程中起重要作用,例如细胞周期调节和多种疾病。 14-3-3蛋白的家庭是一种吸引人的目标,因为它们用作各种蛋白质的结合伙伴,因此能够调节其生物活性。 通过传统的筛查方法发现小分子调节剂,特别是稳定剂,这些复合物是一个具有挑战性的任务。 在此,我们首先将动态组合化学(DCC)应用于PPI靶标,以发现14-3-3蛋白的调节剂。 通过表面等离子体共振(SPR)的DCC实验评价来自DCC实验的增殖实验,显示低微摩尔(K-D15-16μm)酰腙是14-3-3 / Symaptopodin PPI稳定剂。 因此,DCC似乎非常适合发现不仅是调制器的发现,甚至是令人难以置信地挑战PPI的更难以捉摸的稳定剂。

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