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Selective plasmenylcholine oxidation by hypochlorous acid: formation of lysophosphatidylcholine chlorohydrins
Authors:Messner Maria C  Albert Carolyn J  Hsu Fong-Fu  Ford David A
Affiliation:a Department of Biochemistry and Molecular Biology, St. Louis University Health Sciences Center, St. Louis, MO 63104, United States
b Department of Internal Medicine, Washington University, St. Louis, MO 63110, United States
Abstract:The plasmalogen sn-1 vinyl ether bond is targeted by hypochlorous acid (HOCl) produced by activated phagocytes. In the present study, the attack of the plasmalogen sn-1 vinyl ether bond by HOCl is shown to be preferred compared to the attack of double bonds present in the sn-2 position aliphatic chain (sn-2 alkenes) of both plasmenylcholine and phosphatidylcholine. Lysophosphatidylcholine (LPC) is a product from the initial HOCl attack of plasmenylcholine and the sn-2 alkene bonds present in this LPC product are secondary targets of HOCl leading to the production of LPC-chlorohydrins (ClOH). The aliphatic ClOH was demonstrated in both the positive and negative ion mode using collisionally-activated dissociation (CAD) of the molecular ion of LPC-ClOH. Furthermore, HOCl treatment of endothelial cells led to the preferential attack of plasmalogens in comparison to that of diacyl choline glycerophospholipids. Taken together, plasmenylcholine is oxidized preferentially over phosphatidylcholine and leads to the production of LPC-ClOH.
Keywords:GPC, sn-glycero-3-phosphorylcholine   GC-MS, gas chromatography-mass spectrometry   GC-FID, gas chromatography flame ionization detection   TLC, thin layer chromatography   PFB-Br, pentafluorobenzoyl bromide   α-ClFALD, α-chloro-fatty aldehydes   2-ClHDA, 2-chlorohexadecanal   LPC, lysophosphatidylcholine   pPOPC, 1-O-hexadec-1&prime  -enyl-2-octadec-9&prime  -enoyl-GPC   POPC, 1-hexadecanoyl-2-octadec-9&prime  -enoyl-GPC   ClOH, chlorohydrin   ESI-MS, electrospray ionization-mass spectrometry   CAD, collisionally-activated dissociation   RCS, reactive chlorinating species   SRM, selected reaction monitoring   HCAEC, human coronary artery endothelial cells
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