Exploring the effect of inhibitor AKB‐9778 on VE‐PTP by molecular docking and molecular dynamics simulation

Abstract Diabetic macular edema, also known as diabetic eye disease, is mainly caused by the overexpression of vascular endothelial protein tyrosine phosphatase (VE‐PTP) at hypoxia/ischemic. AKB‐9778 is a known VE‐PTP inhibitor that can effectively interact with the active site of VE‐PTP to inhibit the activity of VE‐PTP. However, the binding pattern of VE‐PTP with AKB‐9778 and the dynamic implications of AKB‐9778 on VE‐PTP system at the molecular level are poorly understood. Through molecular docking, it was found that the AKB‐9778 was docked well in the binding pocket of VE‐PTP by the interactions of hydrogen bond and Van der Waals. Furthermore, after molecular dynamic simulations on VE‐PTP system and VE‐PTP AKB‐9778 system, a series of postdynamic analyses found that the flexibility and conformation of the active site undergone an obvious transition after VE‐PTP binding with AKB‐9778. Moreover, by constructing the RIN, it was found that the different interactions in the active site were the detailed reasons for the conformational differences between these two systems. Thus, the finding here might provide a deeper understanding of AKB‐9778 as VE‐PTP Inhibitor.