Elsevier

Methods in Enzymology

Volume 35, 1975, Pages 396-425
Methods in Enzymology

[47] Thin-layer chromatography of neutral glycosphingolipids

https://doi.org/10.1016/0076-6879(75)35178-1Get rights and content

Publisher Summary

This chapter describes the methods for separation by thin layer chromatography of glycosphingolipids that do not contain sialic acid and are called neutral glycosphingolipids. These glycosphingolipids include not only genuine neutral glycosphingolipids but also sulfatides, psychosines, and ceramides. The successful separation of neutral glycosphingolipids performed on lipid samples enriched with glycosphingolipids is dependent upon the quality of enriched samples. If enriched samples represent pure, or almost pure, fractions of neutral glycosphingolipids, their separations can be achieved without difficulty by using silica gel chromatoplates and a chloroform–methanol–water mixture as the developing solvent, usually used for separation of glycosphingolipids. The type of silica gel, the composition of enriched samples, and the nature of the research problem will determine the ratio of ingredients in the above-mentioned developing solvent.

Reference (73)

  • FolchJ. et al.

    J. Biol. Chem.

    (1957)
  • SkipskiV.P. et al.

    J. Lipid Res.

    (1967)
  • NeskovicN.M. et al.

    J. Chromatogr.

    (1970)
  • NeskovicN. et al.

    Clin. Chim. Acta

    (1972)
  • EberleinK. et al.

    J. Chromatogr.

    (1971)
  • SkipskiV.P. et al.

    Biochim. Biophys. Acta

    (1967)
  • LepageM.

    J. Chromatogr.

    (1964)
  • SvennerholmE. et al.

    Biochim. Biophys. Acta

    (1963)
  • WrightR.S.

    J. Chromatogr.

    (1971)
  • BischelM.D. et al.

    Biochim. Biophys. Acta

    (1963)
  • SvennerholmL.

    Biochim. Biophys. Acta

    (1957)
  • VaskovskyV.E. et al.

    J. Chromatogr.

    (1972)
  • DittmerJ.C. et al.

    J. Lipid Res.

    (1964)
  • VaskovskyV.E. et al.

    J. Lipid Res.

    (1968)
  • SkipskiV.P. et al.

    Arch. Biochem. Biophys.

    (1959)
  • VanceD.E. et al.

    J. Lipid Res.

    (1967)
  • SvennerholmE. et al.

    Biochim. Biophys. Acta

    (1963)
  • KatesM.
  • SaitoT. et al.

    J. Lipid Res.

    (1971)
  • HakomoriS. et al.

    Biochim. Biophys. Acta

    (1970)
  • HakomoriS.

    Chem. Phys. Lipids

    (1970)
  • EsselmanW.J. et al.

    J. Biol. Chem.

    (1973)
  • GahmbergC.G. et al.

    J. Biol. Chem.

    (1973)
  • DesnickR.J. et al.

    J. Lipid Res.

    (1970)
  • KopaczykK.C. et al.

    J. Lipid Res.

    (1965)
  • SuzukiK. et al.

    J. Lipid Res.

    (1967)
  • TaoR.V.P. et al.

    Biochim. Biophys. Acta

    (1970)
  • YangH. et al.

    J. Biol. Chem.

    (1971)
  • YoungO.M. et al.

    J. Chromatogr.

    (1965)
  • KeanE.L.

    J. Lipid Res.

    (1966)
  • GattS.

    J. Neurochem.

    (1965)
  • SpenceM.W. et al.

    J. Neurochem.

    (1967)
  • SuzukiK.

    J. Neurochem.

    (1965)
  • C. Entenman, Vol. 3...
  • N. S. Radin, Vol. 14...
  • V. P. Skipski and M. Barclay, Vol. 14...
  • Cited by (138)

    • Altered lipid synthesis by lack of yeast Pah1 phosphatidate phosphatase reduces chronological life span

      2015, Journal of Biological Chemistry
      Citation Excerpt :

      Mitochondrial phospholipids were separated on silica gel plates by two-dimensional TLC (60). The separated lipids were stained with primulin (61), subjected to fluoroimaging, and quantified with ImageQuant software. The identity of phospholipids was confirmed by comparison with standards.

    • Characterization of the mucilage extracted from jaracatiá (Carica quercifolia (A. St. Hil.) Hieron)

      2015, Carbohydrate Polymers
      Citation Excerpt :

      Microorganisms with development potential in food were used: one species being Gram positive (Staphylococcus aureus ATCC 25923) and the other Gram negative (Escherichia coli ATCC 25992), acquired from the Oswaldo Cruz Foundation (Fiocruz), Rio de Janeiro/RJ. After hydrolysis, the monosaccharides mixture was analyzed by TLC on 10 cm silica-gel Plate 60 (Merck) using ethyl acetate:acetic acid:n-propanol:water (4:2:2:1, v v−1) as mobile phase and developed with orcinol-sulfuric acid (Sassaki, Souza, Cipriani & Iacomini, 2008; Skipski, 1875). The standards used for TLC were: rhamnose (Rha), arabinose (Ara), galactose (Gal), glucose (Glc), galacturonic acid (GalA) and glucuronic acid (GlcA)

    View all citing articles on Scopus
    View full text