School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, PR China.
School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, PR China.
J Chromatogr A. 2020 May 24;1619:460948. doi: 10.1016/j.chroma.2020.460948. Epub 2020 Feb 5.
In this study, an online capillary electrophoresis (CE) based dual-enzyme (thrombin and factor Xa) co-immobilized microreactor (THR-FXa IMER) was constructed for studying enzyme kinetics and screening dual-target inhibitors against THR and FXa with the aid of the polydopamine/graphene oxide (PDA/GO) coating. Based on the developed THR-FXa IMER, the Michaelis-Menten constants (K) of THR and FXa were calculated to be 187.26 and 48.80 μM, respectively. The inhibition constants (K) for two known inhibitors, argatroban and rivaroxaban, on THR and FXa were determined to be 14.73 and 0.41 nM, respectively. In addition, after 30 consecutive runs, the enzymes' activity was remained 98% of the initial immobilized activity for both THR and FXa, which shows that the constructed IMER has good stability and repeatability. Finally, the developed method was successfully applied to screen dual-target inhibitors against THR and FXa from 30 small molecular compounds. Among them, 10 compounds such as salvianolic acid C and epigallocatechin gallate (EGCG) have dual-enzyme inhibitory activity, and 2 compounds named saikosaponin A and oleuropein have single THR inhibitory activity, 5 compounds such as rosemary acid and salvianolic acid B have single FXa inhibitory activity. Finally, the molecular interactions between enzyme and potential inhibitors were further verified via the molecular docking, and a new compound with a theoretically good coagulation inhibition effect was designed by the scaffold hopping study. In summary, the developed THR-FXa IMER is a reliable method for screening THR and/or FXa inhibitors.
在这项研究中,构建了一种基于在线毛细管电泳(CE)的双重酶(凝血酶和因子 Xa)共固定化微反应器(THR-FXa IMER),借助聚多巴胺/氧化石墨烯(PDA/GO)涂层研究酶动力学并筛选针对 THR 和 FXa 的双靶抑制剂。基于开发的 THR-FXa IMER,计算出 THR 和 FXa 的米氏常数(K)分别为 187.26 和 48.80 μM。两种已知抑制剂(argatroban 和 rivaroxaban)对 THR 和 FXa 的抑制常数(K)分别为 14.73 和 0.41 nM。此外,在 30 次连续运行后,两种酶的活性仍保持初始固定化活性的 98%,这表明构建的 IMER 具有良好的稳定性和重现性。最后,该方法成功用于从 30 种小分子化合物中筛选针对 THR 和 FXa 的双靶抑制剂。其中,10 种化合物,如丹参酸 C 和表没食子儿茶素没食子酸酯(EGCG)具有双重酶抑制活性,2 种化合物,如柴胡皂苷 A 和橄榄苦苷,具有单一的 THR 抑制活性,5 种化合物,如迷迭香酸和丹酚酸 B,具有单一的 FXa 抑制活性。最后,通过分子对接进一步验证了酶与潜在抑制剂之间的分子相互作用,并通过骨架跳跃研究设计了一种具有理论上良好凝血抑制效果的新化合物。总之,开发的 THR-FXa IMER 是一种可靠的筛选 THR 和/或 FXa 抑制剂的方法。