| Literature DB >> 31140688 |
Tristan de Rond1,2,3, Jian Gao4, Amin Zargar2, Markus de Raad4,5, Jack Cunha2, Trent R Northen2,4,5, Jay D Keasling1,2,6,7,8.
Abstract
Assaying for enzymatic activity is a persistent bottleneck in biocatalyst and drug development. Existing high-throughput assays for enzyme activity tend to be applicable only to a narrow range of biochemical transformations, whereas universal enzyme characterization methods usually require chromatography to determine substrate turnover, greatly diminishing throughput. We present an enzyme activity assay that allows the high-throughput mass-spectrometric detection of enzyme activity in complex matrices without the need for a chromatographic step. This technology, which we call probing enzymes with click-assisted NIMS (PECAN), can detect the activity of medically and biocatalytically significant cytochrome P450s in cell lysate, microsomes, and bacteria. Using this approach, a cytochrome P450BM3 mutant library was successfully screened for the ability to catalyze the oxidation of the sesquiterpene valencene.Entities:
Keywords: biocatalysis; cytochrome P450; enzyme assays; high-throughput screening; mass spectrometry
Year: 2019 PMID: 31140688 PMCID: PMC6640108 DOI: 10.1002/anie.201901782
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336