Carlesso Antonio, Chintha Chetan, Gorman Adrienne M, Samali Afshin, Eriksson Leif A
Department of Chemistry and Molecular Biology, University of Gothenburg, 405 30 Göteborg, Sweden.
Apoptosis Research Centre, National University of Ireland Galway, H91 TK33 Galway, Ireland.
ACS Omega. 2018 Oct 31;3(10):13313-13322. doi: 10.1021/acsomega.8b01404. Epub 2018 Oct 16.
Inositol-requiring enzyme 1 (IRE1) is an orchestrator of the unfolded protein response (UPR), the cellular response to endoplasmic reticulum (ER) stress that plays a crucial role in tumor development. IRE1 signaling is the most evolutionary conserved branch of the UPR. Under ER stress, the IRE1 luminal domain undergoes a conformational change to multimerize, resulting in trans-autophosphorylation and activation of the cytosolic kinase and endoribonuclease domain. Adenosine triphosphate-competitive inhibitors that bind to the IRE1 kinase site can modulate the activity of the RNase domain through an allosteric relationship between the IRE1 kinase and RNase domains. The current study aims at the investigation of available structural data of the IRE1 kinase domain and provides insights into the design of novel kinase inhibitors. To this end, a detailed analysis of IRE1 kinase active site and investigation of suitable structures for virtual screening studies were performed. The results indicate in silico target fishing as an appropriate strategy for the identification of novel IRE1 kinase binders, further validating the robustness of the in silico protocol. Importantly, the study highlights the kinase-inhibiting RNase attenuator (KIRA)-bound protein data bank 4U6R structure as the best protein structure to perform virtual screening to develop diverse and more potent KIRA-like IRE1 kinase inhibitors that are capable of allosterically affecting the RNase activity.
肌醇需求酶1(IRE1)是未折叠蛋白反应(UPR)的协调者,UPR是细胞对内质网(ER)应激的反应,在肿瘤发展中起关键作用。IRE1信号通路是UPR中进化上最保守的分支。在内质网应激下,IRE1的腔结构域发生构象变化形成多聚体,导致胞质激酶和核糖核酸内切酶结构域的反式自磷酸化和激活。与IRE1激酶位点结合的三磷酸腺苷竞争性抑制剂可通过IRE1激酶和核糖核酸酶结构域之间的变构关系调节核糖核酸酶结构域的活性。本研究旨在调查IRE1激酶结构域的现有结构数据,并为新型激酶抑制剂的设计提供见解。为此,对IRE1激酶活性位点进行了详细分析,并对用于虚拟筛选研究的合适结构进行了调查。结果表明,计算机辅助靶点筛选是鉴定新型IRE1激酶结合物的合适策略,进一步验证了计算机辅助方案的稳健性。重要的是,该研究强调了与激酶抑制性核糖核酸酶衰减剂(KIRA)结合的蛋白质数据库4U6R结构是进行虚拟筛选以开发能够变构影响核糖核酸酶活性且多样且更有效的类KIRA IRE1激酶抑制剂的最佳蛋白质结构。