Persico Marco, Di Dato Antonio, Orteca Nausicaa, Fattorusso Caterina, Novellino Ettore, Andreoli Mirko, Ferlini Cristiano
Department of Pharmacy, University of Napoli "Federico II", Via D. Montesano 49, 80131 Napoli, Italy.
Curr Top Med Chem. 2015;15(20):2019-31. doi: 10.2174/1568026615666150519102257.
The majority of functionally important biological processes are regulated by allosteric communication within individual proteins and across protein complexes. The proteins controlling these communication networks respond to changes in the cellular environment by switching between different conformational states. Targeting the interface residues mediating these processes through the rational identification of molecules modulating or mimicking their effects holds great therapeutic potential. Protein-protein interactions (PPIs) have shown to have a high degree of plasticity since they occur through small regions, called hot spots, which are included in binding surfaces or in binding clefts of the proteins and are characterized by a high degree of complementarity. This prompted several researchers to compare the protein structure to human grammar proposing terms like "protein language". The decoding of this language represent a new paradigm not only to clarify the dynamics of many biological processes but also to improve the opportunities in drug discovery. In this review, we try to give an overview on intra-molecular and inter-molecular protein communication mechanisms describing the protein interaction domains (PIDs) and short linear motifs (SLiMs), which delineate the authentic syntactic and semantic units in a protein. Moreover, we illustrate some novel approaches performed on natural compounds and on synthetic derivatives aimed at developing new classes of potential drugs able to interfere with intra-molecular and inter-molecular protein communication.
大多数具有重要功能的生物过程是由单个蛋白质内部以及蛋白质复合物之间的变构通讯调控的。控制这些通讯网络的蛋白质通过在不同构象状态之间切换来响应细胞环境的变化。通过合理识别调节或模拟其作用的分子来靶向介导这些过程的界面残基具有巨大的治疗潜力。蛋白质-蛋白质相互作用(PPI)已显示出高度的可塑性,因为它们通过称为热点的小区域发生,这些热点包含在蛋白质的结合表面或结合裂隙中,其特征是具有高度互补性。这促使一些研究人员将蛋白质结构与人类语法进行比较,提出了“蛋白质语言”等术语。解读这种语言不仅代表了一种新的范式,以阐明许多生物过程的动态,还代表了改善药物发现机会的新范式。在本综述中,我们试图概述分子内和分子间蛋白质通讯机制,描述蛋白质相互作用结构域(PID)和短线性基序(SLiM),它们描绘了蛋白质中真正的句法和语义单元。此外,我们举例说明了一些针对天然化合物和合成衍生物进行的新方法,旨在开发能够干扰分子内和分子间蛋白质通讯的新型潜在药物。