2. Academic Validation
  3. Characterization of covalent binding of tyrosine kinase inhibitors to plasma proteins

Characterization of covalent binding of tyrosine kinase inhibitors to plasma proteins

  • Drug Metab Pharmacokinet. 2020 Oct;35(5):456-465. doi: 10.1016/j.dmpk.2020.07.002.
Xiaoyun Liu 1,  Dan Feng 2,  Mingyue Zheng 1,  Yongmei Cui 3,  Dafang Zhong 4
Affiliations

Affiliations

  • 1 State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • 2 State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China; Department of Chemistry, Shanghai University, Shanghai, 200444, China.
  • 3 Department of Chemistry, Shanghai University, Shanghai, 200444, China.
  • 4 State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China; University of Chinese Academy of Sciences, Beijing, 100049, China. Electronic address: dfzhong@simm.ac.cn.
PMID: 32847720 DOI: 10.1016/j.dmpk.2020.07.002
Abstract

Eight covalent tyrosine kinase inhibitors (TKIs) were investigated to determine the characteristics of their covalent binding to plasma proteins. The data revealed that their covalent binding to plasma proteins is of species difference. In addition to the reports on neratinib and pyrotinib, osimertinib, alflutinib, AST5902, and ibrutinib were confirmed to covalently bind to the Lys-190 of human serum albumin (HSA). Molecular docking was used to simulate the binding mode of TKIs to HSA. The results exhibited the non-covalent interactions between covalent TKIs and HSA, which stabilize the TKIs-HSA complex and explain the selectivity of covalent binding. The t1/2 values of TKIs that are covalently bound to HSA or human plasma proteins were studied in vitro, and the features highly correlated with the t1/2 were determined by quantitative calculations and linear modeling. Reversibility of the covalent binding and the factors affecting the process of reversibility were evaluated. In conclusion, acrylamide moiety of covalent TKIs can covalently bind to lysine residue of HSA, most of which were determined to be Lys-190. The covalent binding is of species difference, especially between animal and human. Except for osimertinib, covalent binding between TKIs and HSA are reversible.

Keywords

Covalent binding; Covalent tyrosine kinase inhibitors; Human serum albumin; Linear modeling; Molecular docking; Quantitative calculations; Species difference.

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