Carbohydrate moieties of molluscan Rapana venosa hemocyanin

被引:16
|
作者
Dolashka-Angelova, P [1 ]
Beck, A
Dolashki, A
Stevanovic, S
Beltramini, M
Salvato, B
Hristova, R
Velkova, L
Voelter, W
机构
[1] Bulgarian Acad Sci, Inst Organ Chem, Sofia, Bulgaria
[2] Univ Tubingen, Univ Kliniken, Klin Chem Zentral Lab, Tubingen, Germany
[3] Univ Tubingen, Phys Biochem Abt, Inst Physiol Chem, Tubingen, Germany
[4] Univ Tubingen, Inst Cell Biol, Dept Immunol, Tubingen, Germany
[5] Univ Padua, Dept Biol, Padua, Italy
[6] Univ Padua, CNR, Inst Biomed Technol, Padua, Italy
关键词
D O I
10.1016/j.micron.2003.10.032
中图分类号
TH742 [显微镜];
学科分类号
摘要
Using Zn2+ ions as new method, several FUs have been isolated from molluscan He Rapana venosa wihtout formation of non-functional proteolytic side products. N-terminal sequences of these fragments in comparison with FUS from other gastropodan Hcs show a very high degree of structural identity. Four Fus, purified from enzyme-treated structural subunits RvH1 and RvH2 (RvH1-a, RvH1-f, RvH2-a and RvH2-e) show identical N-terminal sequences compared to fragments isolated after treatment with Zn2+ ions. However, in some cases trypsin cleaves RvH chains at different positions if compared to the Zn2+ treatment. To analyze the oligosaccharide composition of two FUS from the first structural subunit of Rapana He, RvH1-a and RvH1-f, several techniques were applied: capillary electrophoresis, MALDI-MS, ESI-MS in combination with glycosidase digestions. On basis of these results and the determined amino acid sequence two N-linkage sites were identified in the FU RvH1-a, but only one in the FU RvH1-f. (C) 2003 Elsevier Ltd. All rights reserved.
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收藏
页码:101 / 104
页数:4
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