Structure of the glycosylphosphatidylinositol membrane anchor glycan of a class-2 variant surface glycoprotein from Trypanosoma brucei
Structure of the glycosylphosphatidylinositol membrane anchor glycan of a class-2 variant surface glycoprotein from Trypanosoma brucei
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DOI:
10.1006/jmbi.1997.1600
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发表时间:
1998-03-27
影响因子:
5.6
通讯作者:
Ferguson, MAJ
中科院分区:
文献类型:
--
作者:
Mehlert, A;Richardson, JM;Ferguson, MAJ
The neutral glycan fraction of the glycosylphosphatidylinositol (GPI) membrane anchor of a class-2 variant surface glycoprotein (VSG) from Trypanosoma brucei was isolated following aqueous hydrogen fluoride dephosphorylation and nitrous acid deamination of the purified glycoprotein. The neutral glycans were fractionated by high-pH anion exchange chromatography and gel-filtration and six major glycan structures were solved by a combination of one and two-dimensional NMR, composition analysis, methylation linkage analysis and electrospray-mass spectrometry. The glycans were similar to those previously described for class-1 VSGs, in that they contained the linear trimannosyl sequence Man alpha 1-2Man alpha 1-6Man and a complex alpha-galactose branch of up to Gal alpha 1-2Gal alpha 1-6(Gal alpha 1-2)Gal, but most also contained an additional galactose residue attached alpha 1-2 to the non-reducing terminal mannose residue and about one-third contained an additional galactose residue attached beta 1-3 to the middle mannose residue. The additional complexity of the class-2 VSG GPI glycans is discussed in terms of a biosynthetic model that explains the full range of mature GPI structures that can be expressed on different VSG classes by the same trypanosome clone. (C) 1998 Academic Press Limited.