Freites J Alfredo, Tobias Douglas J
Department of Chemistry, University of California, Irvine, 1102 Natural Sciences 2, Irvine, California 92697-2025, United States.
J Phys Chem B. 2024 Aug 8;128(31):7577-7585. doi: 10.1021/acs.jpcb.4c03015. Epub 2024 Jul 25.
Aquaporin 0 (AQP0) plays a key role in water circulation in the eye lens through a variety of functions. In contrast to mammalian genomes, zebrafish contains two genes leading to a separation of AQP0 multiple functions between the two gene products, Aqp0a and Aqp0b. A notable feature of the zebrafish AQP0 paralogs is the increased water permeability of Aqp0b relative to Aqp0a as well as a severa lfold increase relative to mammalian AQP0. Here, we report equilibrium molecular dynamics (MD) simulations on the microsecond timescale to identify the structural basis underlying the differences in water permeability between zebrafish AQP0 paralogs and between AQP0 mammalian and fish orthologs. Our simulations are able to reproduce the experimental trends in water permeability. Our results suggest that a substitution of a key Y23 residue in mammalian AQP0 for F23 in fish AQP0 orthologs introduces significant changes in the conformational dynamics of the CS-I structural motif, which, in conjunction with different levels of hydration of the channel vestibule, can account for the differences in permeabilities between fish and mammalian AQP0 orthologs and between zebrafish AQP0 paralogs.
水通道蛋白0(AQP0)通过多种功能在晶状体的水循环中发挥关键作用。与哺乳动物基因组不同,斑马鱼含有两个基因,导致AQP0的多种功能在两种基因产物Aqp0a和Aqp0b之间分离。斑马鱼AQP0旁系同源物的一个显著特征是,相对于Aqp0a,Aqp0b的水通透性增加,并且相对于哺乳动物AQP0增加了几倍。在这里,我们报告了在微秒时间尺度上的平衡分子动力学(MD)模拟,以确定斑马鱼AQP0旁系同源物之间以及AQP0哺乳动物和鱼类直系同源物之间水通透性差异的结构基础。我们的模拟能够重现水通透性的实验趋势。我们的结果表明,哺乳动物AQP0中的关键Y23残基被鱼类AQP0直系同源物中的F23取代,会导致CS-I结构基序的构象动力学发生显著变化,这与通道前庭不同程度的水化作用一起,可以解释鱼类和哺乳动物AQP0直系同源物之间以及斑马鱼AQP0旁系同源物之间通透性的差异。