Li Deng, Minkara Mona S
Department of Bioengineering, Northeastern University, Boston, Massachusetts 02120, United States.
J Chem Inf Model. 2024 Dec 23;64(24):9459-9473. doi: 10.1021/acs.jcim.4c01361. Epub 2024 Oct 8.
Accurate computational simulations of protein-glycan dynamics are crucial for a comprehensive understanding of critical biological mechanisms, including host-pathogen interactions, immune system defenses, and intercellular communication. The accuracy of these simulations, including molecular dynamics (MD) simulation and alchemical free energy calculations, critically relies on the appropriate parameters, including the water model, because of the extensive hydrogen bonding with glycan hydroxyl groups. However, a systematic evaluation of water models' accuracy in simulating protein-glycan interaction at the molecular level is still lacking. In this study, we used full atomistic MD simulations and alchemical absolute binding free energy (ABFE) calculations to investigate the performance of five distinct water models in six protein-glycan complex systems. We evaluated water models' impact on structural dynamics and binding affinity through over 5.8 μs of simulation time per system. Our results reveal that most protein-glycan complexes are stable in the overall structural dynamics regardless of the water model used, while some show obvious fluctuations with specific water models. More importantly, we discover that the stability of the binding motif's conformation is dependent on the water model chosen when its residues form weak hydrogen bonds with the glycan. The water model also influences the conformational stability of the glycan in its bound state according to density functional theory (DFT) calculations. Using alchemical ABFE calculations, we find that the OPC water model exhibits exceptional consistency with experimental binding affinity data, whereas commonly used models such as TIP3P are less accurate. The findings demonstrate how different water models affect protein-glycan interactions and the accuracy of binding affinity calculations, which is crucial in developing therapeutic strategies targeting these interactions.
蛋白质-聚糖动力学的精确计算模拟对于全面理解关键生物学机制至关重要,这些机制包括宿主-病原体相互作用、免疫系统防御和细胞间通讯。由于与聚糖羟基广泛形成氢键,这些模拟(包括分子动力学(MD)模拟和炼金术自由能计算)的准确性严重依赖于包括水模型在内的适当参数。然而,在分子水平上对水模型模拟蛋白质-聚糖相互作用准确性的系统评估仍然缺乏。在本研究中,我们使用全原子MD模拟和炼金术绝对结合自由能(ABFE)计算来研究六种蛋白质-聚糖复合系统中五种不同水模型的性能。我们通过每个系统超过5.8微秒的模拟时间评估了水模型对结构动力学和结合亲和力的影响。我们的结果表明,无论使用何种水模型,大多数蛋白质-聚糖复合物在整体结构动力学上都是稳定的,而有些则在特定水模型下表现出明显的波动。更重要的是,我们发现当结合基序的残基与聚糖形成弱氢键时,其构象的稳定性取决于所选择的水模型。根据密度泛函理论(DFT)计算,水模型还会影响聚糖在其结合状态下的构象稳定性。使用炼金术ABFE计算,我们发现OPC水模型与实验结合亲和力数据具有出色的一致性,而常用模型如TIP3P则不太准确。这些发现证明了不同的水模型如何影响蛋白质-聚糖相互作用以及结合亲和力计算的准确性,这对于开发针对这些相互作用的治疗策略至关重要。