Thomas Jemima C, Cooper Jonathan M, Clayton Natasha S, Wang Chensu, White Michael A, Abell Chris, Owen Darerca, Mott Helen R
From the Department of Biochemistry, University of Cambridge, Cambridge CB2 1GA, United Kingdom, Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, United Kingdom.
Department of Cell Biology, UT Southwestern Medical Center, Dallas, Texas 75390-9039.
J Biol Chem. 2016 Aug 26;291(35):18310-25. doi: 10.1074/jbc.M116.720243. Epub 2016 Jun 22.
Aberrant Ras signaling drives numerous cancers, and drugs to inhibit this are urgently required. This compelling clinical need combined with recent innovations in drug discovery including the advent of biologic therapeutic agents, has propelled Ras back to the forefront of targeting efforts. Activated Ras has proved extremely difficult to target directly, and the focus has moved to the main downstream Ras-signaling pathways. In particular, the Ras-Raf and Ras-PI3K pathways have provided conspicuous enzyme therapeutic targets that were more accessible to conventional drug-discovery strategies. The Ras-RalGEF-Ral pathway is a more difficult challenge for traditional medicinal development, and there have, therefore, been few inhibitors reported that disrupt this axis. We have used our structure of a Ral-effector complex as a basis for the design and characterization of α-helical-stapled peptides that bind selectively to active, GTP-bound Ral proteins and that compete with downstream effector proteins. The peptides have been thoroughly characterized biophysically. Crucially, the lead peptide enters cells and is biologically active, inhibiting isoform-specific RalB-driven cellular processes. This, therefore, provides a starting point for therapeutic inhibition of the Ras-RalGEF-Ral pathway.
异常的Ras信号传导驱动着众多癌症,因此迫切需要能够抑制这种信号传导的药物。这种迫切的临床需求,再加上药物研发领域的最新创新,包括生物治疗药物的出现,使得Ras重新成为靶向治疗努力的前沿焦点。事实证明,直接靶向激活的Ras极具难度,因此研究重点已转向主要的下游Ras信号通路。特别是,Ras-Raf和Ras-PI3K信号通路提供了引人注目的酶治疗靶点,这些靶点更易于采用传统的药物研发策略。对于传统药物开发而言,Ras-RalGEF-Ral信号通路是一个更具挑战性的难题,因此,报道的能够破坏该信号轴的抑制剂很少。我们利用Ral效应蛋白复合物的结构作为设计和表征α-螺旋钉肽的基础,这些肽能选择性地结合活性GTP结合型Ral蛋白,并与下游效应蛋白竞争。这些肽已通过生物物理方法进行了全面表征。至关重要的是,先导肽能够进入细胞并具有生物活性,可抑制异构体特异性RalB驱动的细胞过程。因此,这为治疗性抑制Ras-RalGEF-Ral信号通路提供了一个起点。