Department of Pharmacoinformatics, National Institute of Pharmaceutical Education and Research, S.A.S. Nagar, Punjab, India.
PLoS One. 2018 Jun 18;13(6):e0199020. doi: 10.1371/journal.pone.0199020. eCollection 2018.
Protein tyrosine phosphatase 1B (PTP1B) is a validated therapeutic target for Type 2 diabetes due to its specific role as a negative regulator of insulin signaling pathways. Discovery of active site directed PTP1B inhibitors is very challenging due to highly conserved nature of the active site and multiple charge requirements of the ligands, which makes them non-selective and non-permeable. Identification of the PTP1B allosteric site has opened up new avenues for discovering potent and selective ligands for therapeutic intervention. Interactions made by potent allosteric inhibitor in the presence of PTP1B were studied using Molecular Dynamics (MD). Computationally optimized models were used to build separate pharmacophore models of PTP1B and TCPTP, respectively. Based on the nature of interactions the target residues offered, a receptor based pharmacophore was developed. The pharmacophore considering conformational flexibility of the residues was used for the development of pharmacophore hypothesis to identify potentially active inhibitors by screening large compound databases. Two pharmacophore were successively used in the virtual screening protocol to identify potential selective and permeable inhibitors of PTP1B. Allosteric inhibition mechanism of these molecules was established using molecular docking and MD methods. The geometrical criteria values confirmed their ability to stabilize PTP1B in an open conformation. 23 molecules that were identified as potential inhibitors were screened for PTP1B inhibitory activity. After screening, 10 molecules which have good permeability values were identified as potential inhibitors of PTP1B. This study confirms that selective and permeable inhibitors can be identified by targeting allosteric site of PTP1B.
蛋白酪氨酸磷酸酶 1B(PTP1B)是 2 型糖尿病的一个经过验证的治疗靶点,因为它作为胰岛素信号通路的负调节剂具有特定作用。由于活性位点高度保守和配体的多种电荷要求,发现活性位点定向的 PTP1B 抑制剂非常具有挑战性,这使得它们是非选择性和不可渗透的。鉴定 PTP1B 的变构位点为发现用于治疗干预的有效且选择性的配体开辟了新途径。使用分子动力学(MD)研究了在存在 PTP1B 的情况下,有效变构抑制剂的相互作用。使用计算优化的模型分别构建了 PTP1B 和 TCPTP 的独立药效团模型。基于目标残基提供的相互作用性质,开发了基于受体的药效团。考虑到残基构象灵活性的药效团用于开发药效团假设,通过筛选大型化合物数据库来鉴定潜在的活性抑制剂。两个药效团相继用于虚拟筛选方案,以鉴定潜在的选择性和可渗透的 PTP1B 抑制剂。使用分子对接和 MD 方法确定了这些分子的变构抑制机制。几何标准值证实了它们稳定 PTP1B 处于开放构象的能力。鉴定为潜在抑制剂的 23 种分子被筛选以评估它们对 PTP1B 的抑制活性。筛选后,确定了 10 种具有良好渗透性值的分子作为 PTP1B 的潜在抑制剂。这项研究证实,通过靶向 PTP1B 的变构位点,可以鉴定出选择性和可渗透的抑制剂。