9vci

Publication Abstract from PubMed

The escalating threat of antibiotic resistance poses a critical challenge to global public health, necessitating the urgent development of novel therapeutic agents with distinct mechanisms of action and unique structural scaffolds. Tryptophanyl-tRNA synthetase (TrpRS) has emerged as a promising antibacterial target. Our previous study demonstrated that the clinically utilized Bruton's tyrosine kinase (BTK) inhibitor tirabrutinib, along with several of its analogues, can simultaneously occupy both the substrates l-Trp and tRNA(Trp) A76 binding sites of Escherichia coli tryptophanyl-tRNA synthetase (EcTrpRS), thereby effectively inhibiting its catalytic activity. Building on this finding, we employed structure-based drug design to systematically optimize the interactions of tirabrutinib analogues with the l-Trp and tRNA(Trp) binding sites, as well as to further extend the structure to the adjacent ATP binding site within the catalytic pocket of EcTrpRS to establish additional interactions, leading to the design and synthesis of 22 new derivatives. Among these, WRS22 (a racemic mixture) demonstrated the best binding to EcTrpRS, with a DeltaT(m) value of 33.2 degrees C and 90 % inhibition rate at 10 muM concentration. Its binding affinity for EcTrpRS (K(d) = 0.33 +/- 0.03 muM) is superior to that of the positive control, indolmycin (K(d) = 0.71 +/- 0.1 muM). Notably, WRS22 displayed no affinity to human cytoplasmic TrpRS (HcTrpRS) and its interaction with human BTK is likely to be disrupted, indicating high degree of target selectivity. Therefore, the structure-guided design successfully developed new tirabrutinib analogues as inhibitors of bacterial TrpRS, presenting a promising lead compound for the development of AARS-based antibacterial agents.

Structure-based design of tirabrutinib derivatives as inhibitors of bacterial tryptophanyl-tRNA synthetase.,Xia K, Peng X, Xiao L, Huang Q, Xu J, Chen B, Zhou H Bioorg Chem. 2025 Sep 9;165:108978. doi: 10.1016/j.bioorg.2025.108978. PMID:40945024^[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.