A Covalent Cysteine-Targeting Kinase Inhibitor of Ire1 Permits Allosteric Control of Endoribonuclease Activity

作者：Waller Daniel D^*; Jansen Gregor; Golizeh Makan; Martel Lorion Chloe; Dejgaard Kurt; Shiao Tze Chieh; Mancuso John; Tsantrizos Youla S; Roy Rene; Sebag Michael; Sleno Lekha; Thomas David Y

来源：ChemBioChem, 2016, 17(9): 843-851.

DOI：10.1002/cbic.201500485

• endoplasmic reticulum stress
• enzyme catalysis
• inhibitors
• Ire1
• type IV kinase inhibitor
• Xbp1

The unfolded protein response (UPR) initiated by the transmembrane kinase/ribonuclease Ire1 has been implicated in a variety of diseases. Ire1, with its unique position in the UPR, is an ideal target for the development of therapies; however, the identification of specific kinase inhibitors is challenging. Recently, the development of covalent inhibitors has gained great momentum because of the irreversible deactivation of the target. We identified and determined the mechanism of action of the Ire1-inhibitory compound UPRM8. MS analysis revealed that UPRM8 inhibition occurs by covalent adduct formation at a conserved cysteine at the regulatory DFG+2 position in the Ire1 kinase activation loop. Mutational analysis of the target cysteine residue identified both UPRM8-resistant and catalytically inactive Ire1 mutants. We describe a novel covalent inhibition mechanism of UPRM8, which can serve as a lead for the rational design and optimization of inhibitors of human Ire1.

• 出版日期2016-5-3