Aim: To study the comparative molecular interactions of Thymol and Imatinib with the active sites of Breakpoint Cluster Region (BCR)-Abelson (ABL) fusion protein using molecular docking analysis for the selective anti-Chronic myeloid leukemia (CML) activity. Materials and Methods: In this study, Group 1 is binding affinity of Imatinib with BCR-ABL Fusion Protein and Group 2 is binding affinity of Thymol with BCR-ABL Fusion Protein. The sample size was calculated with pretest power 80%. The sample size per group is 10 and total sample size is 20. The protein structure of BCR-ABL fusion protein was collected from the protein data bank (PDB) website and the ligand structures were collected from the NCBI-PUBCHEM website. The binding energy (kcal/mol) was calculated using Autodock Vina Software. Results: The mean binding affinity of Imatinib (-10.4 kcal/mol) was significantly (p=<0.001, p<0.001, 2-tailed t-test) higher than Thymol (-6.89 kcal/mol) towards the active sites of BCR-ABL fusion protein. Conclusion: In Spite of lesser binding affinity of Thymol compared to Imatinib, Thymol can make strong hydrogen bond and hydrophobic interactions with the aminoacid residues at the active sites of BCR-ABL fusion protein. It suggests that, thymol may bind selectively to the cells of CML and inhibit their proliferation and can act as novel Anti-CML agent.
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