Department of Bioinformatics, Sathyabama Institute of Science and Technology, Chennai, India.
Department of Biotechnology, Sathyabama Institute of Science and Technology, Chennai, India.
Mol Divers. 2024 Aug;28(4):2563-2581. doi: 10.1007/s11030-023-10695-7. Epub 2023 Jul 19.
Phosphoinositide kinases (PIKs) are a type of lipid kinase that acts as an upstream activator of oncogenic signaling. Presently accessible therapeutic compounds have downsides, such as toxicity and dubious efficacy, as well as lengthy treatment durations, which have bred resistance. Here we attempt to screen the Indian Ocean-derived red algal compounds to be used as a promising lead for PI3Kα inhibitor development. Experimental structure of the PI3K alpha Isoform-Specific Inhibitor alpelisib complex-based pharmacophore model was constructed and used as key to mark off the suitable lead compounds from the pool of marine-derived red algal compounds of Indian Ocean. Besides, the study encompasses pharmacophore scaffold screening as well as physicochemical and pharmacokinetic parameter assessment. We employed molecular docking and molecular dynamics simulation to assess the binding type and stability of 21 red algal derivatives. Twelve compounds demonstrated a sustained binding mode within the PI3Kα binding pocket with an optimal protein backbone root-mean-square deviation, also prompted hydrogen bonding throughout the simulations, and also implies that these MNPs have firmly mediated the interaction with prime hinge region residues in the PI3Kα ATP binding pocket. DFT studies revealed that proposed compounds had the greatest occupied molecular orbital electrophilicity index, basicity, and dipole moment, all of which attributed their stability as well as binding affinity at the PI3Kα active site. Our study's findings revealed that CMNPD31054, CMNPD4798, CMNPD27861, CMNPD4799, CMNPD27860, CMNPD9533, CMNPD3732, CMNPD4221, CMNPD31058, CMNPD31052, CMNPD29281, and CMNPD31055 can be used as lead compounds for PI3KΑ isoform inhibitors design.
磷酸肌醇激酶(PIKs)是一种脂质激酶,作为致癌信号的上游激活剂发挥作用。目前可获得的治疗化合物存在毒性和疗效可疑以及治疗时间长等缺点,这些缺点导致了耐药性的产生。在这里,我们试图筛选印度洋来源的红藻化合物,将其作为开发 PI3Kα 抑制剂的有前途的先导化合物。基于 PI3K alpha 同工型特异性抑制剂 alpelisib 复合物的实验结构构建了药效团模型,并将其用作从印度洋来源的海洋衍生红藻化合物库中标记合适的先导化合物的关键。此外,该研究还包括药效团骨架筛选以及物理化学和药代动力学参数评估。我们采用分子对接和分子动力学模拟来评估 21 种红藻衍生物的结合类型和稳定性。有 12 种化合物在 PI3Kα 结合口袋中表现出持续的结合模式,具有最佳的蛋白质骨架均方根偏差,并且在整个模拟过程中也能诱导氢键,这表明这些 MNPs 已经牢固地介导了与 PI3Kα ATP 结合口袋中的主要铰链区域残基的相互作用。DFT 研究表明,所提出的化合物具有最大占据分子轨道电负性指数、碱性和偶极矩,所有这些都归因于它们在 PI3Kα 活性部位的稳定性和结合亲和力。我们的研究结果表明,CMNPD31054、CMNPD4798、CMNPD27861、CMNPD4799、CMNPD27860、CMNPD9533、CMNPD3732、CMNPD4221、CMNPD31058、CMNPD31052、CMNPD29281 和 CMNPD31055 可以用作 PI3KΑ 同工型抑制剂设计的先导化合物。