| Literature DB >> 26119262 |
Ahmed E Fouda1, Mary Kay H Pflum2.
Abstract
ATP analogues have been powerful compounds for the study of kinase-catalyzed phosphorylation. However, the cell impermeability of ATP analogues has largely limited their use to in vitro lysate-based experiments. Herein, we report the first cell-permeable ATP analogue, ATP-polyamine-biotin (APB). APB is shown to promote biotin labeling of kinase substrates in live cells and has future applications in phosphoprotein purification and analysis. More generally, these studies provide a foundation for the development of additional cell-permeable ATP analogues for cell-signaling research.Entities:
Keywords: ATP; biotinylation; cell permeability; enzymes; kinases
Mesh:
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Year: 2015 PMID: 26119262 PMCID: PMC4551444 DOI: 10.1002/anie.201503041
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336