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Proteome-wide Ligand and Target Discovery by Using Strain-Enabled Cyclopropane Electrophiles

Yue Liu, Zhongtang Yu, Peishan Li, Tao Yang, Ke Ding, Zhimin Zhang, Yi Tan, Zhengqiu Li

2024Journal of the American Chemical Society18 citationsDOI

Abstract

The evolving use of covalent ligands as chemical probes and therapeutic agents could greatly benefit from an expanded array of cysteine-reactive electrophiles for efficient and versatile proteome profiling. Herein, to expand the current repertoire of cysteine-reactive electrophiles, we developed a new class of strain-enabled electrophiles based on cyclopropanes. Proteome profiling has unveiled that C163 of lactate dehydrogenase A (LDHA) and C88 of adhesion regulating molecule 1 (ADRM1) are ligandable residues to modulate the protein functions. Moreover, fragment-based ligand discovery (FBLD) has revealed that one fragment ( Y-35 ) shows strong reactivity toward C66 of thioredoxin domain-containing protein 12 (TXD12), and its covalent binding has been demonstrated to impact its downstream signal pathways. TXD12 plays a pivotal role in enabling Y-35 to exhibit its antisurvival and antiproliferative effects. Finally, dicarbonitrile-cyclopropane has been demonstrated to be an electrophilic warhead in the development of GSTO1-involved dual covalent inhibitors, which is promising to alleviate drug resistance.

Topics & Concepts

ChemistryCyclopropaneElectrophileProteomeStrain (injury)Ligand (biochemistry)Computational biologyDrug discoveryStereochemistryCombinatorial chemistryBiochemistryOrganic chemistryReceptorRing (chemistry)CatalysisInternal medicineBiologyMedicineCyclopropane Reaction MechanismsClick Chemistry and ApplicationsCatalytic Alkyne Reactions
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