Institute for Advanced Study, Shenzhen University, Shenzhen 518060, China.
College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen 518060, China.
Int J Mol Sci. 2021 Jan 25;22(3):1164. doi: 10.3390/ijms22031164.
Recent studies have identified cyclic GMP-AMP synthase (cGAS) as an important target for treating autoimmune diseases, and several inhibitors of human cGAS (hcGAS) and their structures in complexation with hcGAS have been reported. However, the mechanisms via which these inhibitors interact with hcGAS are not completely understood. Here, we aimed to assess the performance of molecular mechanics/Poisson-Boltzmann solvent-accessible surface area (MM/PBSA) in evaluating the binding affinity of various hcGAS inhibitors and to elucidate their detailed interactions with hcGAS from an energetic viewpoint. Using molecular dynamics (MD) simulation and MM/PBSA approaches, the estimated free energies were in good agreement with the experimental ones, with a Pearson's correlation coefficient and Spearman's rank coefficient of 0.67 and 0.46, respectively. In per-residue energy decomposition analysis, four residues, K362, R376, Y436, and K439 in hcGAS were found to contribute significantly to the binding with inhibitors via hydrogen bonding, salt bridges, and various π interactions, such as π· · ·π stacking, cation· · ·π, hydroxyl· · ·π, and alkyl· · ·π interactions. In addition, we discussed other key interactions between specific residues and ligands, in particular, between H363 and JUJ, F379 and 9BY, and H437 and 8ZM. The sandwiched structures of the inhibitor bound to the guanidinium group of R376 and the phenyl ring of Y436 were also consistent with the experimental data. The results indicated that MM/PBSA in combination with other virtual screening methods, could be a reliable approach to discover new hcGAS inhibitors and thus is valuable for potential treatments of cGAS-dependent inflammatory diseases.
最近的研究已经确定环鸟苷酸-腺苷酸合酶(cGAS)是治疗自身免疫性疾病的重要靶点,并且已经报道了几种人 cGAS(hcGAS)抑制剂及其与 hcGAS 复合物的结构。然而,这些抑制剂与 hcGAS 相互作用的机制尚未完全清楚。在这里,我们旨在评估分子力学/泊松-玻尔兹曼溶剂可及表面积(MM/PBSA)在评估各种 hcGAS 抑制剂结合亲和力方面的性能,并从能量角度阐明它们与 hcGAS 的详细相互作用。使用分子动力学(MD)模拟和 MM/PBSA 方法,估计的自由能与实验值吻合良好,Pearson 相关系数和 Spearman 秩系数分别为 0.67 和 0.46。在残基能量分解分析中,发现 hcGAS 中的四个残基 K362、R376、Y436 和 K439 通过氢键、盐桥和各种π相互作用(如π···π堆积、阳离子···π、羟基···π 和烷基···π 相互作用)对与抑制剂的结合有显著贡献。此外,我们还讨论了特定残基与配体之间的其他关键相互作用,特别是 H363 与 JUJ、F379 与 9BY 和 H437 与 8ZM 之间的相互作用。抑制剂与 R376 的胍基和 Y436 的苯环结合的夹心结构也与实验数据一致。结果表明,结合其他虚拟筛选方法的 MM/PBSA 可能是发现新的 hcGAS 抑制剂的可靠方法,因此对于 cGAS 依赖性炎症性疾病的潜在治疗具有重要价值。