Schistosoma mansoni: Radiometric assay of lectin binding specificities of the major egg glycoprotein and its carbohydrate-rich fragment

Sara Lustigman*, Joseph Hamburger

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

The binding by lectins of the Schistosoma mansoni major egg glycoprotein and of a carbohydrate-rich fragment which is serologically crossreactive with it was studied. The major egg glycoprotein was purified from a crude soluble egg antigen by a succession of affinity chromatography procedures on concanavalin A-sepharose and by ion-exchange chromatography. The carbohydrate-rich fragment was isolated by ultrafiltration of the crude glycoprotein fraction initially obtained from the crude soluble egg antigens. The major egg glycoprotein and the carbohydrate-rich fragment contain 77 and 92.5% carbohydrate, respectively. When radioiodinated and run on SDS-polyacrylamide gel electrophoresis, each of them exhibited a single peak with respective Rf values of 0.33 and 1.0, and their respective molecular weights were 70K and 10-13K. The binding of the radioiodinated major egg glycoprotein and the carbohydrate-rich fragment by peanut agglutinin, Ricinus communis agglutinin-60, wheat germ agglutinin, and lotus agglutinin was studied by double diffusion in agar, and by a radiometric solid-phase assay in which the lectins were used to coat microtiter plates. The latter assay was employed to determine the specificity of the binding by inhibition with the specific sugars. Both the major egg glycoprotein and the carbohydrate-rich fragment bound specifically to concanavalin A columns as indicated by their isolation procedure. They also bound specifically to peanut agglutinin, R. communis agglutinin 60, and lotus agglutinin, while binding by wheat germ agglutinin appeared not to be specific. Thus, the major egg glycoprotein and the carbohydrate-rich fragment appear to possess the following similar terminal sugars: mannose and/or glucose (concanavalin A specific); galactose (peanut agglutinin and R. communis agglutinin-60 specific) and/or N-acetylgalactosamine (R. communis-60 agglutinin specific) and/or galactose-N-acetylgalactosamine (peanut agglutinin specific); fucose (lotus agglutinin specific).

Original languageEnglish
Pages (from-to)59-67
Number of pages9
JournalExperimental Parasitology
Volume59
Issue number1
DOIs
StatePublished - Feb 1985

Keywords

  • Blood fluke
  • Schistosoma mansoni
  • Trematode
  • digenetic

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