Institute of Pharmacy, Department of Medicinal Chemistry, Martin-Luther-University Halle-Wittenberg, W.-Langenbeck-Str. 4, 06120 Halle, Germany.
Institute of Pharmacy, Department of Pharmacology, Martin-Luther-University Halle-Wittenberg, W.-Langenbeck-Str. 4, 06120 Halle, Germany.
Bioorg Med Chem. 2018 Aug 7;26(14):4014-4024. doi: 10.1016/j.bmc.2018.06.027. Epub 2018 Jun 20.
As a member of the Wee-kinase family protein kinase PKMYT1 is involved in G/M checkpoint regulation of the cell cycle. Recently, a peptide microarray approach led to the identification of a small peptide; EFS as substrate of PKMYT1, which allowed for subsequent development of an activity assay. The developed activity assay was used to characterize the PKMYT1 catalyzed phosphorylation of EFS. For the first time kinetic parameters for PKMYT1, namely K, K and v were determined. The optimized assay was used to screen the published protein kinase inhibitor sets (PKIS I and II), two sets of small molecule ATP-competitive kinase inhibitors reported by GlaxoSmithKline. We identified ten inhibitors, providing different scaffolds. The inhibitors were further characterized by using binding assay, activity and functional assay. In addition, docking studies were carried out in order to rationalize the observed biological activities. The derived results provide the basis for further chemical optimization of PKMYT1 inhibitors and for further analysis of PKMYT1 as target for anti-cancer therapy.
作为 Wee-kinase 家族蛋白激酶家族的一员,PKMYT1 参与细胞周期的 G/M 检查点调控。最近,一种肽微阵列方法鉴定出一种小分子 EFS 是 PKMYT1 的底物,随后开发了一种活性测定法。所开发的活性测定法用于表征 PKMYT1 催化的 EFS 磷酸化。首次确定了 PKMYT1 的动力学参数,即 K、K 和 v。优化后的测定法用于筛选已发表的蛋白激酶抑制剂集(PKIS I 和 II)和葛兰素史克报道的两组合成小分子 ATP 竞争性激酶抑制剂。我们鉴定了十种抑制剂,提供了不同的支架。使用结合测定法、活性和功能测定法进一步对抑制剂进行了表征。此外,还进行了对接研究,以合理化观察到的生物学活性。得出的结果为进一步化学优化 PKMYT1 抑制剂以及进一步分析 PKMYT1 作为抗癌治疗靶标提供了基础。