MSDC-0160和MSDC-0602与人线粒体丙酮酸载体(MPC) 1和2异源二聚体的结合

C. Phelix, Allen K. Bourdon, Jason L. Dugan, G. Villareal, George Perry
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引用次数: 1

摘要

线粒体丙酮酸载体(MPC)是治疗阿尔茨海默病、帕金森病、糖尿病和非酒精性脂肪性肝炎(NASH)的新靶点。代谢解决方案开发公司(MSDC)有两种噻唑烷二酮,MSDC-0160和MSDC-0602,正在筹备中。本文描述了MPC1/2异源二聚体同源性模型的结果。从UniProt中获取MPC1和MPC2的FASTA序列,并将其提交给RaptorX,从而获得各自的最佳候选单体“蛋白质数据库”文件。MPC1的一种突变体L36I也被处理。这些被提交给PyDock以生成最佳候选MPC1/2异源二聚体模型,用于AutoDock Vina和“Rosetta Online Server that Includes Everyone”(ROSIE)的配体对接分析。在MPC1和MPC2亚基上都发现了丙酮酸和两种药物的多个结合位点,除了L36I突变转运体的中间和开放状态外,每种情况下药物的亲和力几乎是两倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MSDC-0160 and MSDC-0602 Binding with Human Mitochondrial Pyruvate Carrier (MPC) 1 and 2 Heterodimer
The mitochondrial pyruvate carrier (MPC) is a novel target for therapeutic drugs to treat Alzheimer's and Parkinson's disease, diabetes mellitus, and non-alcoholic steatohepatitis (NASH). Metabolic Solutions Development Company (MSDC) has two thiazolidinediones, MSDC-0160 and MSDC-0602, in the pipeline. This report describes results for a MPC1/2 heterodimer homology model. The FASTA sequences for MPC1 and MPC2 were accessed from UniProt and submitted to RaptorX, resulting in best candidate monomeric “protein data base” files for each. One mutant form of MPC1, L36I, was also processed. These were submitted to PyDock to generate best candidate MPC1/2 heterodimer models that were used for ligand docking analyses with AutoDock Vina and “Rosetta Online Server that Includes Everyone” (ROSIE). Multiple binding sites for pyruvate and both drugs were found on both MPC1 and MPC2 subunits with drugs having nearly double the affinity in each case except the intermediate and open-in states for the L36I mutant transporter.
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