Abstract

Aminopropyl silica gel was prepared from porous silica gel and was used as a solid support for immunoadsorbent in the purification of anti-glycolipid antibodies. For neutral glycosphingolipids, a carboxyl function was generated by oxidation of the olefinic double bond of the sphingosine moiety, whereas for gangliosides the carboxyl group of sialic acid was used to couple with aminopropyl silica gel in the presence of a carbodiimide. These compounds were used for purifying anti-glycolipid antibodies from serum of immunized rabbits. The antibodies bound to the su-strate were released by 2 M potassium thiocyanate and their immunological properties were studied. Aminopropyl silica gel may be preferred over conventional organic solid supports for the following reasons: 1) faster flow rate; 2) higher capacity; 3) easier handling; 4) more economical; and 5) lower susceptibility to microbial attack.

Highlights

  • Aminopropyl silica gel was prepared from porous silica gel and was used as a solid support for immunoadsorbentin the purification of anti-glycolipidantibodies

  • We describe the preparation of aminopropyl silica gel and its application in the preparation of glycolipid immunoadsorbents which were utilized in purifying anti-glycolipid antibodies

  • A comparative study between aminopropyl silica gel and other conventional organic supports was made: the results indicated that the former was preferable

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Summary

Introduction

Aminopropyl silica gel was prepared from porous silica gel and was used as a solid support for immunoadsorbentin the purification of anti-glycolipidantibodies. The glycolipid-acidsfrom ceramide trihexoside, globoside, paragloboside, Forssman glycolipid, GM1, and native gangliosides, viz. GM3, GD3, GMl, GDl,, GDlb, and GTlb, were coupled to aminopropyl silica gel.

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