Strategic Design of Catalytic Lysine‐Targeting Reversible Covalent BCR‐ABL Inhibitors. Issue 31 (24th June 2021)

• Record Type: Journal Article
• Authors: Quach, David; Tang, Guanghui; Anantharajan, Jothi; Baburajendran, Nithya; Poulsen, Anders; Wee, John L. K.; Retna, Priya; Li, Rong; Liu, Boping; Tee, Doris H. Y.; Kwek, Perlyn Z.; Joy, Joma K.; Yang, Wan‐Qi; Zhang, Chong‐Jing; Foo, Klement; Keller, Thomas H.; Yao, Shao Q.
• Is Part Of: Angewandte Chemie international edition. Volume 60:Issue 31(2021)
• Page Start: 17131
• Page End: 17137
• Publication Date: 2021-06-24
• Subjects: cancer -- covalent inhibitors -- lysine -- proteomics -- reversibility; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.202105383
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: Targeted covalent inhibitors have re‐emerged as validated drugs to overcome acquired resistance in cancer treatment. Herein, by using a carbonyl boronic acid (CBA) warhead, we report the structure‐based design of BCR‐ABL inhibitors via reversible covalent targeting of the catalytic lysine with improved potency against both wild‐type and mutant ABL kinases, especially ABL T315I bearing the gatekeeper residue mutation. We show the evolutionarily conserved lysine can be targeted selectively, and the selectivity depends largely on molecular recognition of the non‐covalent pharmacophore in this class of inhibitors, probably due to the moderate reactivity of the warhead. We report the first co‐crystal structures of covalent inhibitor‐ABL kinase domain complexes, providing insights into the interaction of this warhead with the catalytic lysine. We also employed label‐free mass spectrometry to evaluate off‐targets of our compounds at proteome‐wide level in different mammalian cells. Abstract : Using iminoboronate chemistry, we report the first successful examples of catalytic lysine‐targeting reversible covalent BCR‐ABL inhibitors which inhibited both ABL WT and ABL T315I at nanomolar potency. We also demonstrated how the study of off‐targets for this class of compounds could be performed using activity‐based protein profiling and mass spectrometry.