Mehran Mohammadpour saray - Department of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran,Iran
Zahra Hajihassan - Department of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran,Iran

Background and Aim: T cell immunoglobulin and mucin-domain containing-۳ (TIM-۳) is a type I transmembrane protein that plays a key role in regulating innate and adaptive immune responses in infections, autoimmune diseases, and tumors by binding to its ligands especially (CEACAM۱) and inhibiting Th۱ responses and the expression of cytokines such as TNF and INF-γ. Therefore, this receptor and its ligand are increasingly being considered as a target for numerous therapeutics that are under clinical development. In this study, the extracellular region of CEACAM۱ was mutated with bioinformatics tools to increase its binding affinity for its receptor (TIM-۳). As this engineered protein will bind to TIM-۳, natural ligand (CEACAM۱) cannot bind to the TIM-۳ in the cell membrane. As a result, TIM-۳ will not activate and T-cell will not be inhibited so the progression of autoimmune and inflammatory diseases and cancer will stop.Methods: The CEACAM۱ sequence was mutated by the R software. Interaction of each mutant to TIM-۳ was investigated by HADDOCK server and the binding energy was calculated by FoldX software.Results: Among the ۱۰۰ mutants of CEACAM۱, the mutant containing the Y۳۴K point mutation was the best mutant because it had the lowest binding energy and highest binding affinity relative to natural CEACAM۱.Conclusion: This engineered protein had lower binding energy than wild-type protein, so it could bind more strongly to TIM-۳ protein.

TIM-۳, CEACAM۱, Docking, FoldX