Synthesis and intermembrane transfer of pyrene-labelled liponucleotides: ceramide phosphothymidines

Abstract

Phospholipid conjugates of 3′-azido-3′-deoxythymidine (AZT) show activity against human immunodeficiency virus (HIV) in vitro. Here we report on the synthesis and characterization of two pyrene containing conjugates: 2- N-(4-(pyren-1-yl)butanoyl)ceramide 5′-phosphothymidine (Pbs–Cer–P–T) (XII) and 2- N-(10-(pyren-1-yl)decanoyl)ceramide 5′-phosphothymidine (Pds–Cer–P–T) (XIII). These fluorescent labelled conjugates served as model compounds to study incorporation of sphingoliponucleotides into membranes. The complex compounds were prepared by condensation of 3′-acetylthymidine and labelled ceramides using the phosphite triester coupling procedure. UV absorption, fluorimetry as well as 1H-, 31P-, 13C-NMR analyses were used for structure confirmation of the synthesized substances. When incorporated into small unilamellar 1-palmitoyl-2-oleoyl-glycerophosphatidylcholine (POPC) vesicles and incubated with unlabelled acceptor POPC vesicles, the compounds (XII) and (XIII) exhibited spontaneous transfer. Kinetic data suggest that transfer from donor to acceptor vesicles occurred via the intervening aqueous phase. The non-specific lipid transfer protein from bovine liver stimulated the transfer of Pds–Cer–P–T between phospholipid vesicles in a concentration dependent manner.