Department of Physiology, School of Medicine, Ajou University, Suwon 16499, Korea.
Department of Molecular Science and Technology, Ajou University, Suwon 16499, Korea.
Biomolecules. 2021 May 27;11(6):798. doi: 10.3390/biom11060798.
Glutamate dehydrogenase (GDH) is a ubiquitous enzyme that catalyzes the reversible oxidative deamination of glutamate to α-ketoglutarate. It acts as an important branch-point enzyme between carbon and nitrogen metabolisms. Due to the multifaceted roles of GDH in cancer, hyperinsulinism/hyperammonemia, and central nervous system development and pathologies, tight control of its activity is necessitated. To date, several GDH structures have been solved in its closed form; however, intrinsic structural information in its open and apo forms are still deficient. Moreover, the allosteric communications and conformational changes taking place in the three different GDH states are not well studied. To mitigate these drawbacks, we applied unbiased molecular dynamic simulations (MD) and network analysis to three different GDH states i.e., apo, active, and inactive forms, for investigating their modulatory mechanisms. In this paper, based on MD and network analysis, crucial residues important for signal transduction, conformational changes, and maps of information flow among the different GDH states were elucidated. Moreover, with the recent findings of allosteric modulators, an allosteric wiring illustration of GDH intramolecular signal transductions would be of paramount importance to obtain the process of this enzyme regulation. The structural insights gained from this study will pave way for large-scale screening of GDH regulators and could support researchers in the design and development of new and potent GDH ligands.
谷氨酸脱氢酶(GDH)是一种普遍存在的酶,能够催化谷氨酸的可逆氧化脱氨反应,生成α-酮戊二酸。它作为碳氮代谢之间的一个重要分支点酶发挥作用。由于 GDH 在癌症、高胰岛素血症/高氨血症和中枢神经系统发育及病变中的多种作用,需要严格控制其活性。迄今为止,已经解决了几种 GDH 结构的封闭形式;然而,其开放和无配体形式的内在结构信息仍然不足。此外,三种不同 GDH 状态下的变构通讯和构象变化尚未得到很好的研究。为了克服这些缺点,我们应用无偏分子动力学模拟(MD)和网络分析来研究三种不同的 GDH 状态,即无配体、活性和无活性形式,以研究它们的调节机制。在本文中,基于 MD 和网络分析,阐明了对于信号转导、构象变化以及不同 GDH 状态之间信息流的关键残基。此外,鉴于最近发现的变构调节剂,对于获得该酶调节过程的 GDH 分子内信号转导的变构接线图将是至关重要的。这项研究获得的结构见解将为大规模筛选 GDH 调节剂铺平道路,并为研究人员设计和开发新的有效的 GDH 配体提供支持。