Max-Planck-Institut für molekulare Physiologie, Otto-Hahn-Str. 11, D-44227 Dortmund, Germany.
Biol Chem. 2019 Dec 18;401(1):143-163. doi: 10.1515/hsz-2019-0330.
Since its discovery as an oncogene more than 40 years ago, Ras has been and still is in the focus of many academic and pharmaceutical labs around the world. A huge amount of work has accumulated on its biology. However, many questions about the role of the different Ras isoforms in health and disease still exist and a full understanding will require more intensive work in the future. Here we try to survey some of the structural findings in a historical perspective and how it has influenced our understanding of structure-function and mechanistic relationships of Ras and its interactions. The structures show that Ras is a stable molecular machine that uses the dynamics of its switch regions for the interaction with all regulators and effectors. This conformational flexibility has been used to create small molecule drug candidates against this important oncoprotein.
自 40 多年前发现它作为致癌基因以来,Ras 一直是全世界许多学术和制药实验室的关注焦点。在其生物学方面已经积累了大量的工作。然而,关于不同 Ras 同工型在健康和疾病中的作用仍有许多问题尚待解决,而全面了解 Ras 及其相互作用的结构-功能和机制关系需要今后更加深入的研究。在这里,我们尝试从历史的角度来调查一些结构发现,以及这些发现如何影响我们对 Ras 及其相互作用的结构-功能和机制关系的理解。这些结构表明,Ras 是一种稳定的分子机器,它利用其开关区域的动力学与所有调节剂和效应子相互作用。这种构象灵活性已被用于开发针对这种重要致癌蛋白的小分子药物候选物。