Fischer Gerhard, Rossmann Maxim, Hyvönen Marko
Department of Biochemistry, University of Cambridge, 80 Tennis Court Road, Cambridge CB2 1GA, UK.
Department of Biochemistry, University of Cambridge, 80 Tennis Court Road, Cambridge CB2 1GA, UK.
Curr Opin Biotechnol. 2015 Dec;35:78-85. doi: 10.1016/j.copbio.2015.04.006. Epub 2015 May 15.
Protein-protein interactions (PPI) have become increasingly popular drug targets, with a number of promising compounds currently in clinical trials. Recent research shows, that PPIs can be modulated in more ways than direct inhibition, where novel non-competitive modes of action promise a solution for the difficult nature of PPI drug discovery. Here, we review recently discovered PPI modulators in light of their mode of action and categorise them as disrupting versus stabilising, orthosteric versus allosteric and by their ability to affect the proteins' dynamics. We also give recent examples of compounds successful in the clinic, analyse their physicochemical properties and discuss how to overcome the hurdles in discovering alternative modes of modulation.
蛋白质-蛋白质相互作用(PPI)已成为越来越受欢迎的药物靶点,目前有许多有前景的化合物正处于临床试验阶段。最近的研究表明,PPI的调节方式比直接抑制更多样,新型非竞争性作用模式有望解决PPI药物发现的难题。在此,我们根据其作用模式对最近发现的PPI调节剂进行综述,并将它们分为破坏型与稳定型、正构型与别构型,以及根据它们影响蛋白质动力学的能力进行分类。我们还给出了近期在临床中取得成功的化合物实例,分析了它们的物理化学性质,并讨论了如何克服发现替代调节模式过程中的障碍。