Abstract
Hamster liver 14C-mannolipid, prepared by DEAE-cellulose chromatography of the organic extract, is shown to be a more efficient donor of mannose to endogenous glycoproteins then guanosine-diphosphate-mannose. Analysis of endogenous acceptors after proteolysis reveals that several compounds separated by DEAE-sephadex chromatography are labeled by both 14C-mannolipid and GDP-mannose 14C.
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