Aleem Muhammad Tahir, Lakho Shakeel Ahmed, Mohsin Muhammad, Ul Haq Shahbaz, Ali Ashiq, Huang Danmei, Gao Fenfei
Department of Pharmacology, Shantou University Medical College, Shantou, 515041, China.
Center for Gene Regulation in Health and Disease, Department of Biological, Geological, and Environmental Sciences, College of Sciences and Health Professions, Cleveland State University, Cleveland, OH, 44115, USA.
Biochem Biophys Rep. 2025 May 5;42:102031. doi: 10.1016/j.bbrep.2025.102031. eCollection 2025 Jun.
Trichinellosis, caused by species, including , is a foodborne zoonotic disease. Upon ingestion, ML swiftly invade the intra-multicellular niche of the small intestine, undergoing four rapid molts to mature into adults. In general, the route of transmission for nematodes occurs through ingestion of pork. Therefore, it is crucial to develop a vaccine that can deal with trichinellosis, particularly for humans and pigs. In this study, homology modelling, molecular docking, simulations and molecular mechanics-based scoring (MM/GBSA) are used to investigate the interaction between membrane-associated progesterone receptor component 2 (-MAPRC2) and different steroids hormones. In the most favorable region, 93 amino acid residues (92.1 %) are located, while 7 amino acids (6.9 %) are located in the allowed region, showing that the model with a 93.33 ERRAT quality factor is good quality. The MD simulations were conducted for 50 ns to explore the affinities and stability of four hormones chosen from the docking studies that showed similar binding poses to the control hormone Mifepristone. Simulations showed that the selected hormones were potent Ts-MAPRC2 binders and can act as leads to determine their activity by biophysical assays. Discovery of these five steroid hormones and interactions with Ts-MAPRC2 could lead to new therapies and vaccines for trichinellosis.
旋毛虫病是一种食源性人畜共患病,由包括旋毛虫属在内的多种旋毛虫引起。摄入后,幼虫迅速侵入小肠的细胞内微环境,经过四次快速蜕皮发育为成虫。一般来说,旋毛虫线虫的传播途径是通过摄入猪肉。因此,开发一种能够应对旋毛虫病的疫苗至关重要,尤其是针对人类和猪。在本研究中,采用同源建模、分子对接、模拟和基于分子力学的评分(MM/GBSA)来研究膜相关孕酮受体成分2(Ts-MAPRC2)与不同甾体激素之间的相互作用。在最有利区域定位了93个氨基酸残基(92.1%),而7个氨基酸(6.9%)位于允许区域,表明具有93.33 ERRAT质量因子的模型质量良好。进行了50纳秒的分子动力学模拟,以探索从对接研究中选择的四种激素与对照激素米非司酮具有相似结合构象的亲和力和稳定性。模拟表明,所选激素是强效的Ts-MAPRC2结合剂,可作为先导物通过生物物理测定来确定其活性。发现这五种甾体激素及其与Ts-MAPRC2的相互作用可能会带来针对旋毛虫病的新疗法和疫苗。