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Electrophilic fragment screening using native mass spectrometry to identify covalent probes for surface cysteines

2025/08/29 by Jack W. Klose, Yezhou Yu, Giovanna Di Trapani +3 · 1 voice
Biochemistry, Genetics and Molecular Biology · Chemistry · #Chemical Synthesis and Analysis #Enzyme function and inhibition #Mass Spectrometry Techniques and Applications

paper · pdf · doi:10.1071/ch25081

openalex publication_date 2025/08/29 · openalex created_date 2025/10/10 · openalex updated_date 2026/06/22

Abstract

Covalent chemical probes form a covalent bond with a target protein of interest to elicit an effect and methods to identify and characterise them are needed. We developed a native mass spectrometry (nMS) method to screen an electrophilic covalent fragment library and identified specific novel binders for the surface exposed cysteine residues of carbonic anhydrase III (CA III). The nMS method was extended to determine the site of protein modification and measure simultaneous binding of an active site noncovalent inhibitor and covalent fragment hit, which is not possible with intact denaturing MS. This study demonstrates the utility of using nMS and the advantages when compared to intact denaturing MS for the discovery and characterisation of new covalent ligands.

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