| Literature DB >> 31030513 |
Yadira F Ordóñez1, José Luís Abad1, Mazen Aseeri1, Josefina Casas1,2, Virginie Garcia3, Mireia Casasampere1, Edward H Schuchman4, Thierry Levade3,5, Antonio Delgado1,6, Gemma Triola7, Gemma Fabrias1,2.
Abstract
Acid ceramidase (AC) hydrolyzes ceramides into sphingoid bases and fatty acids. The enzyme is overexpressed in several types of cancer and Alzheimer's disease, and its genetic defect causes different incurable disorders. The availability of a method for the specific visualization of catalytically active AC in intracellular compartments is crucial for diagnosis and follow-up of therapeutic strategies in diseases linked to altered AC activity. This work was undertaken to develop activity-based probes for the detection of AC. Several analogues of the AC inhibitor SABRAC were synthesized and found to act as very potent (two-digit nM range) irreversible AC inhibitors by reaction with the active site Cys143. Detection of active AC in cell-free systems was achieved either by using fluorescent SABRAC analogues or by click chemistry with an azide-substituted analogue. The compound affording the best features allowed the unprecedented labeling of active AC in living cells.Entities:
Year: 2019 PMID: 31030513 DOI: 10.1021/jacs.8b11687
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419