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从近期蛋白质-蛋白质相互作用抑制(2P2I)的成功中得到的化学和结构启示。

Chemical and structural lessons from recent successes in protein-protein interaction inhibition (2P2I).

机构信息

Interactions et Modulateurs de Réponses (UPR3243), Centre National de la Recherche Scientifique (CNRS) & Université de Provence, 31 Chemin Joseph Aiguier, 13402 Marseille cedex 20, France.

出版信息

Curr Opin Chem Biol. 2011 Aug;15(4):475-81. doi: 10.1016/j.cbpa.2011.05.024. Epub 2011 Jun 22.

Abstract

Worldwide research efforts have driven recent pharmaceutical successes, and consequently, the emerging role of Protein-Protein Interactions (PPIs) as drug targets has finally been widely embraced by the scientific community. Inhibitors of these Protein-Protein Interactions (2P2Is or i-PPIs) are likely to represent the next generation of highly innovative drugs that will reach the market over the next decade. This review describes up-to-date knowledge on this particular chemical space, with a specific emphasis on a subset of this ensemble. We also address current structural knowledge regarding both protein-protein and protein-inhibitor complexes, that is, the 2P2I database. Finally, ligand efficiency analyses permit us to relate potency to size and polarity and to discuss the need to co-develop nanoparticle drug delivery systems.

摘要

全球范围内的研究努力推动了最近的制药成功,因此,蛋白质-蛋白质相互作用(PPIs)作为药物靶点的新兴角色终于被科学界广泛接受。这些蛋白质-蛋白质相互作用(2P2Is 或 i-PPIs)抑制剂很可能代表未来十年将推向市场的下一代高度创新药物。本文综述了这一特定化学空间的最新知识,特别强调了这一组合的一个子集。我们还讨论了关于蛋白质-蛋白质和蛋白质-抑制剂复合物的当前结构知识,即 2P2I 数据库。最后,配体效率分析使我们能够将效力与大小和极性联系起来,并讨论共同开发纳米药物递送系统的必要性。

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