Kinetic characterization of mammalian ceramide synthases: determination of K(m) values towards sphinganine

FEBS Lett. 2007 Nov 13;581(27):5289-94. doi: 10.1016/j.febslet.2007.10.018.

Sujoy Lahiri ¹, Hyunmi Lee, Judith Mesicek, Zvi Fuks, Adriana Haimovitz-Friedman, Richard N Kolesnick, Anthony H Futerman

Affiliations

Affiliation

1 Department of Biological Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel.

PMID: 17977534 DOI: 10.1016/j.febslet.2007.10.018

Abstract

Ceramide is a key metabolite in the pathway of sphingolipid biosynthesis. In mammals, ceramide is synthesized by N-acylation of a sphingoid long-chain base by a family of ceramide synthases (CerS), each of which displays a high specificity towards acyl CoAs of different chain lengths. We now optimize a previously-described assay for measuring CerS activity for use upon over-expression of mammalian CerS, and using these conditions, establish the K(m) value of each CerS towards sphinganine. Remarkably, the K(m) values towards sphinganine are all similar, ranging from 2 to 5microM, even for CerS proteins that are able to use more than one acyl CoA for ceramide synthesis (i.e. CerS4). The availability of this assay will permit further accurate characterization of the kinetic parameters of mammalian CerS proteins.

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