| Literature DB >> 30926626 |
Mireia Casasampere1,2, Núria Bielsa1,2, Daniel Riba1, Laura Bassas1, Ruijuan Xu3, Cungui Mao3, Gemma Fabriàs1,4, José-Luis Abad1, Antonio Delgado5,2, Josefina Casas5,4.
Abstract
New fluorogenic ceramidase substrates derived from the N-acyl modification of our previously reported probes (RBM14) are reported. While none of the new probes were superior to the known RBM14C12 as acid ceramidase substrates, the corresponding nervonic acid amide (RBM14C24:1) is an efficient and selective substrate for the recombinant human neutral ceramidase, both in cell lysates and in intact cells. A second generation of substrates, incorporating the natural 2-(N-acylamino)-1,3-diol-4-ene framework (compounds RBM15) is also reported. Among them, the corresponding fatty acyl amides with an unsaturated N-acyl chain can be used as substrates to determine alkaline ceramidase (ACER)1 and ACER2 activities. In particular, compound RBM15C18:1 has emerged as the best fluorogenic probe reported so far to measure ACER1 and ACER2 activities in a 96-well plate format.Entities:
Keywords: ceramides; sphingolipids; substrate; umbelliferone
Mesh:
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Year: 2019 PMID: 30926626 PMCID: PMC6547634 DOI: 10.1194/jlr.D092759
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922