Alkyne lipids as substrates for click chemistry-based in vitro enzymatic assays

• DOI: 10.1194/jlr.d038653
• Publication Date: 2013-05-25T00:13:41Z
• Authors: Anne Gaebler; Robin Milan; Leon Straub; Dominik Hoelper; Lars Kuerschner; Christoph Thiele
• Keywords: 0301 basic medicine; click-labeling; QD415-436; Biochemistry; Substrate Specificity; Mice; 03 medical and health sciences; acyltransferase; fatty acid amide hydrolase; Animals; Humans; Cells, Cultured; Enzyme Assays; Molecular Structure; 1-Acylglycerophosphocholine O-Acyltransferase; lipid substrate; Lipids; click lipid; ceramide synthase; Mice, Inbred C57BL; Kinetics; Alkynes; Click Chemistry; Oxidoreductases; Acyltransferases

Click chemistry is evolving as a powerful tool in biological applications because it allows the sensitive and specific detection of compounds with alkyne or azido groups. Here we describe the use of alkyne lipids as substrates for in vitro enzymatic assays of lipid modifying enzymes. The small alkyne moiety is introduced synthetically at the terminus of the hydrocarbon chain of various substrate lipids. After the assay, the label is click-reacted with the azide-bearing fluorogenic dye 3-azido-7-hydroxycoumarin, followed by the separation of the lipid mix by thin-layer chromatography and fluorescence detection, resulting in high sensitivity and wide-range linearity. Kinetic analyses using alkyne-labeled substrates for lysophosphatidic acid acyltransferases, lysophosphatidylcholine acyltransferases, and ceramide synthases resulted in Michaelis-Menten constants similar to those for radiolabeled or natural substrates. We tested additional alkyne substrates for several hydrolases and acyltransferases in lipid metabolism. In this pilot study we establish alkyne lipids as a new class of convenient substrates for in vitro enzymatic assays.