Berg Angela, Berg Thorsten
Leipzig University, Institute of Organic Chemistry, Johannisallee 29, 04103, Leipzig, Germany.
Chembiochem. 2016 Apr 15;17(8):650-6. doi: 10.1002/cbic.201500580. Epub 2016 Jan 29.
Polo-like kinase 1 (Plk1), a key player in mitosis, is overexpressed in a wide range of tumor types and has been validated as a target for tumor therapy. In addition to its N-terminal kinase domain, Plk1 harbors a C-terminal protein-protein interaction domain, referred to as the polo-box domain (PBD). Because the PBD is unique to the five-member family of polo-like kinases, and its inhibition is sufficient to inhibit the enzyme, the Plk1 PBD is an attractive target for the inhibition of Plk1 function. Although peptide-based inhibitors are invaluable tools for elucidating the nature of the binding interface, small molecules are better suited for the induction of mitotic arrest and apoptosis in tumor cells by Plk1 inhibition. This review describes the considerable progress that has been made in developing small-molecule and peptide-based inhibitors of the Plk1 PBD.
Polo样激酶1(Plk1)是有丝分裂中的关键因子,在多种肿瘤类型中均有过表达,并且已被确认为肿瘤治疗的靶点。除了其N端激酶结构域外,Plk1还含有一个C端蛋白质-蛋白质相互作用结构域,称为polo盒结构域(PBD)。由于PBD是polo样激酶五成员家族所特有的,且对其抑制足以抑制该酶,因此Plk1的PBD是抑制Plk1功能的一个有吸引力的靶点。尽管基于肽的抑制剂是阐明结合界面性质的宝贵工具,但小分子更适合通过抑制Plk1来诱导肿瘤细胞的有丝分裂停滞和凋亡。本文综述了在开发Plk1 PBD的小分子和基于肽的抑制剂方面取得的重大进展。