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Preparation of Phosphatidylserine

Abstract

SEVERAL methods for the preparation1,2 or quantitative isolation3 of phosphatidylserine are now in existence. An investigation of some of the factors involved in the chromatography of phospholipids4,5 revealed the role of H+ ion exchange in the conversion of the salt form to the acidic form of phosphatidylserine on a silicic acid column. The recognition of this phenomenon, which was also indicated by experimental results published afterwards6, led to the development of a so-called silicic acid–‘Hyflo Super Gel’ column in the sodium form. These columns have been used successfully for the preparation of phosphatidylserine of high purity from ox-brain in conjunction with a shortened version of the method of Folch7 for the isolation of phosphatidylserine-rich fractions.

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References

  1. Sakagami, T., Shimojo, T., and Yokoyama, A., J. Biochem. (Tokyo), 46, 1617 (1959).

    Article  CAS  Google Scholar 

  2. Long, C., Shapiro, B., and Staples, D. A., Biochem. J., 85, 251 (1962).

    Article  CAS  Google Scholar 

  3. Rouser, G., O'Brien, J., and Heller, D., J. Amer. Oil Chemists' Soc., 38, 14 (1961).

    Article  CAS  Google Scholar 

  4. Rouser, G., Bauman, A. J., Kritchevsky, G., Heller, D., and O'Brien, J., J. Amer. Oil Chemists' Soc., 38, 544 (1961).

    Article  CAS  Google Scholar 

  5. Rouser, G., Bauman, A. J., Nicolaides, N., and Heller, D., J. Amer. Oil Chemists' Soc., 38, 1 (1961).

    Article  Google Scholar 

  6. Rathbone, L., Biochem. J., 85, 461 (1962).

    Article  CAS  Google Scholar 

  7. Folch, J., J. Biol. Chem., 146, 35 (1942).

    CAS  Google Scholar 

  8. Folch, J., Lees, M., and Sloane-Stanley, G. H., J. Biol. Chem., 226, 497 (1957).

    CAS  PubMed  Google Scholar 

  9. Reed, C. F., Swisher, S. N., Marinetti, G. V., and Eden, E. G., J. Lab. Clin. Med., 56, 281 (1960).

    CAS  PubMed  Google Scholar 

  10. Rathbone, L., Magee, W. L., and Thompson, R. H. S., Biochem. J., 83, 498 (1962).

    Article  CAS  Google Scholar 

  11. Tattrie, N. H., J. Lipid Res., 1, 60 (1959).

    CAS  Google Scholar 

  12. de Haas, G. H., Daemen, F. J. M., and van Deenen, L. L. M., Biochim. Biophys. Acta, 65, 260 (1962).

    Article  CAS  Google Scholar 

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RATHBONE, L., MARONEY, P. Preparation of Phosphatidylserine. Nature 200, 887–888 (1963). https://doi.org/10.1038/200887a0

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