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Journal of Lipid Research
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    • Research Article3

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    • Alvarez-Jarreta, Jorge1
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    • PC3
    • PE3
    • PG3
    • phosphatidylcholine3
    • phosphatidylinositol3
    • phosphatidylserine3
    • PI3
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    • PL2
    • 1-acylglycerol-3-phosphate-O-acyltransferase1
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    • Research Article
      Open Access

      Identification and characterization of LPLAT7 as an sn-1-specific lysophospholipid acyltransferase

      Journal of Lipid Research
      Vol. 63Issue 10100271Published online: August 29, 2022
      • Hiroki Kawana
      • Masaya Ozawa
      • Takeaki Shibata
      • Hirofumi Onishi
      • Yukitaka Sato
      • Kuniyuki Kano
      • and others
      Cited in Scopus: 0
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        The main fatty acids at the sn-1 position of phospholipids (PLs) are saturated or monounsaturated fatty acids such as palmitic acid (C16:0), stearic acid (C18:0), and oleic acid (C18:1) and are constantly replaced, like unsaturated fatty acids at the sn-2 position. However, little is known about the molecular mechanism underlying the replacement of fatty acids at the sn-1 position, i.e., the sn-1 remodeling. Previously, we established a method to evaluate the incorporation of fatty acids into the sn-1 position of lysophospholipids (lyso-PLs).
        Identification and characterization of LPLAT7 as an sn-1-specific lysophospholipid acyltransferase
      • Research Article
        Open Access

        Isomeric lipid signatures reveal compartmentalized fatty acid metabolism in cancer

        Journal of Lipid Research
        Vol. 63Issue 6100223Published online: May 7, 2022
        • Reuben S.E. Young
        • Andrew P. Bowman
        • Kaylyn D. Tousignant
        • Berwyck L.J. Poad
        • Jennifer H. Gunter
        • Lisa K. Philp
        • and others
        Cited in Scopus: 5
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          The cellular energy and biomass demands of cancer drive a complex dynamic between uptake of extracellular FAs and their de novo synthesis. Given that oxidation of de novo synthesized FAs for energy would result in net-energy loss, there is an implication that FAs from these two sources must have distinct metabolic fates; however, hitherto, all FAs have been considered part of a common pool. To probe potential metabolic partitioning of cellular FAs, cancer cells were supplemented with stable isotope-labeled FAs.
          Isomeric lipid signatures reveal compartmentalized fatty acid metabolism in cancer
        • Research Article
          Open Access

          The SARS-CoV2 envelope differs from host cells, exposes procoagulant lipids, and is disrupted in vivo by oral rinses

          Journal of Lipid Research
          Vol. 63Issue 6100208Published online: April 14, 2022
          • Zack Saud
          • Victoria J. Tyrrell
          • Andreas Zaragkoulias
          • Majd B. Protty
          • Evelina Statkute
          • Anzelika Rubina
          • and others
          Cited in Scopus: 9
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            The lipid envelope of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an essential component of the virus; however, its molecular composition is undetermined. Addressing this knowledge gap could support the design of antiviral agents as well as further our understanding of viral-host protein interactions, infectivity, pathogenicity, and innate immune system clearance. Lipidomics revealed that the virus envelope comprised mainly phospholipids (PLs), with some cholesterol and sphingolipids, and with cholesterol/phospholipid ratio similar to lysosomes.
            The SARS-CoV2 envelope differs from host cells, exposes procoagulant lipids, and is disrupted in vivo by oral rinses
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