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Lysine-Targeting Reversible Covalent Inhibitors with Long Residence Time.


ABSTRACT: We report a new reversible lysine conjugation that features a novel diazaborine product and much slowed dissociation kinetics in comparison to the previously known iminoboronate chemistry. Incorporating the diazaborine-forming warhead RMR1 to a peptide ligand gives potent and long-acting reversible covalent inhibitors of the staphylococcal sortase. The efficacy of sortase inhibition is demonstrated via biochemical and cell-based assays. A comparative study of RMR1 and an iminoboronate-forming warhead highlights the significance and potential of modulating bond dissociation kinetics in achieving long-acting reversible covalent inhibitors.

SUBMITTER: Reja RM 

PROVIDER: S-EPMC8928449 | biostudies-literature | 2022 Jan

REPOSITORIES: biostudies-literature

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Lysine-Targeting Reversible Covalent Inhibitors with Long Residence Time.

Reja Rahi M RM   Wang Wenjian W   Lyu Yuhan Y   Haeffner Fredrik F   Gao Jianmin J  

Journal of the American Chemical Society 20220118 3


We report a new reversible lysine conjugation that features a novel diazaborine product and much slowed dissociation kinetics in comparison to the previously known iminoboronate chemistry. Incorporating the diazaborine-forming warhead RMR1 to a peptide ligand gives potent and long-acting reversible covalent inhibitors of the staphylococcal sortase. The efficacy of sortase inhibition is demonstrated via biochemical and cell-based assays. A comparative study of RMR1 and an iminoboronate-forming wa  ...[more]

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