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14-3-3蛋白-蛋白相互作用:从机理理解到小分子稳定作用

14-3-3 Protein-Protein Interactions: From Mechanistic Understanding to Their Small-Molecule Stabilization.

作者信息

Somsen Bente A, Cossar Peter J, Arkin Michelle R, Brunsveld Luc, Ottmann Christian

机构信息

Department of Biomedical Engineering and Institute for Complex Molecular Systems, Laboratory of Chemical Biology, Eindhoven University of Technology, P.O. Box 513, MB Eindhoven, 5600, Eindhoven, The Netherlands.

Department of Pharmaceutical Chemistry and Small Molecule Discovery Center (SMDC), University of California, San Francisco, California, 94143, United States.

出版信息

Chembiochem. 2024 Jul 15;25(14):e202400214. doi: 10.1002/cbic.202400214. Epub 2024 Jun 24.

DOI:10.1002/cbic.202400214
PMID:38738787
Abstract

Protein-protein interactions (PPIs) are of utmost importance for maintenance of cellular homeostasis. Herein, a central role can be found for 14-3-3 proteins. These hub-proteins are known to bind hundreds of interaction partners, thereby regulating their activity, localization, and/or stabilization. Due to their ability to bind a large variety of client proteins, studies of 14-3-3 protein complexes flourished over the last decades, aiming to gain greater molecular understanding of these complexes and their role in health and disease. Because of their crucial role within the cell, 14-3-3 protein complexes are recognized as highly interesting therapeutic targets, encouraging the discovery of small molecule modulators of these PPIs. We discuss various examples of 14-3-3-mediated regulation of its binding partners on a mechanistic level, highlighting the versatile and multi-functional role of 14-3-3 within the cell. Furthermore, an overview is given on the development of stabilizers of 14-3-3 protein complexes, from initially used natural products to fragment-based approaches. These studies show the potential of 14-3-3 PPI stabilizers as novel agents in drug discovery and as tool compounds to gain greater molecular understanding of the role of 14-3-3-based protein regulation.

摘要

蛋白质-蛋白质相互作用(PPI)对于维持细胞内稳态至关重要。在此过程中,14-3-3蛋白发挥着核心作用。这些中枢蛋白已知能结合数百个相互作用伙伴,从而调节它们的活性、定位和/或稳定性。由于其能够结合多种客户蛋白,在过去几十年里,对14-3-3蛋白复合物的研究蓬勃发展,旨在更深入地从分子层面了解这些复合物及其在健康和疾病中的作用。由于它们在细胞内的关键作用,14-3-3蛋白复合物被认为是极具吸引力的治疗靶点,这促使人们去发现这些PPI的小分子调节剂。我们在机制层面讨论了14-3-3介导的对其结合伙伴调控的各种例子,突出了14-3-3在细胞内的多功能和多方面作用。此外,还概述了14-3-3蛋白复合物稳定剂的发展历程,从最初使用的天然产物到基于片段的方法。这些研究表明,14-3-3 PPI稳定剂作为药物发现中的新型药物以及用于更深入从分子层面理解基于14-3-3的蛋白质调控作用的工具化合物具有潜力。

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Molecular glues of the regulatory ChREBP/14-3-3 complex protect beta cells from glucolipotoxicity.调节性ChREBP/14-3-3复合物的分子胶可保护β细胞免受糖脂毒性。
Nat Commun. 2025 Mar 2;16(1):2110. doi: 10.1038/s41467-025-57241-7.
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Discovery of 14-3-3 PPI Stabilizers by Extension of an Amidine-Substituted Thiophene Fragment.通过扩展一个脒基取代的噻吩片段发现 14-3-3 蛋白磷酸酶抑制剂。
Chembiochem. 2024 Jan 2;25(1):e202300636. doi: 10.1002/cbic.202300636. Epub 2023 Nov 17.
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Structure-Based Optimization of Covalent, Small-Molecule Stabilizers of the 14-3-3σ/ERα Protein-Protein Interaction from Nonselective Fragments.
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Nondegradative Synthetic Molecular Glues Enter the Clinic.非降解性合成分子胶进入临床应用。
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Modulation of Protein-Protein Interactions with Molecular Glues in a Synthetic Condensate Platform.在合成凝聚物平台中利用分子胶对蛋白质-蛋白质相互作用进行调控。
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From Tethered to Freestanding Stabilizers of 14-3-3 Protein-Protein Interactions through Fragment Linking.通过片段连接将 14-3-3 蛋白-蛋白相互作用的束缚型稳定器转变为自由型稳定器。
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