On-Chip Preconcentration Microchip Capillary Electrophoresis Based CE-PRM-LIVE for High-Throughput Selectivity Profiling of Deubiquitinase Inhibitors.
He ZhuJ Scott MellorsWai Cheung ChanJ Will ThompsonScott B FicarroIsidoro TavaresAriana S BrattJens DeckerMichael KrauseGary KruppaSara J BuhrlageJarrod A MartoPublished in: Analytical chemistry (2022)
The family of deubiquitinases (DUBs) comprises ∼100 enzymes that cleave ubiquitin from substrate proteins and thereby regulate key aspects of human physiology. DUBs have recently emerged as disease-relevant and chemically tractable, although currently there are no approved DUB-targeting drugs and most preclinical small molecules are low-potency and/or multitargeted. We paired a novel capillary electrophoresis microchip containing an integrated, "on-chip" C18 bed (SPE-ZipChip) with a TMT version of our recently described PRM-LIVE acquisition scheme on a timsTOF Pro mass spectrometer to facilitate rapid activity-based protein profiling of DUB inhibitors. We demonstrate the ability of the SPE-ZipChip to improve proteome coverage of complex samples as well as the quantitation integrity of CE-PRM-LIVE for TMT labeled samples. These technologies provide a platform to accurately quantify competitive binding of covalent and reversible inhibitors in a multiplexed assay that spans 49 endogenous DUBs in less than 15 min.
Keyphrases
- capillary electrophoresis
- high throughput
- mass spectrometry
- single cell
- ms ms
- solid phase extraction
- high resolution
- endothelial cells
- liquid chromatography
- high performance liquid chromatography
- circulating tumor cells
- small molecule
- cancer therapy
- binding protein
- stem cells
- liquid chromatography tandem mass spectrometry
- protein protein
- tandem mass spectrometry
- drug delivery
- anti inflammatory
- pet imaging
- pet ct
- induced pluripotent stem cells
- mesenchymal stem cells
- transcription factor
- loop mediated isothermal amplification
- drug induced