Acharan sulfate, the new glycosaminoglycan from Achatina fulica Bowdich 1822 -: Structural heterogeneity, metabolic labeling and localization in the body, mucus and the organic shell matrix

被引:22
作者
Vieira, TCRG
Costa, A
Salgado, NC
Allodi, S
Valente, AP
Nasciutti, LE
Silva, LCF
机构
[1] Univ Fed Rio de Janeiro, Ctr Ciencias Saude, Dept Bioquim Med, BR-21941590 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Hosp Univ Clementino Fraga Filho, Lab Tecido Conjunt, BR-21941590 Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, Museu Nacl, Lab Malacol, BR-21941590 Rio De Janeiro, Brazil
[4] Univ Fed Rio de Janeiro, Dept Histol & Embryol, BR-21941590 Rio De Janeiro, Brazil
[5] Univ Fed Rio de Janeiro, Ctr Nacl Ressonancia Magnet Nucl Macromol, BR-21941590 Rio De Janeiro, Brazil
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2004年 / 271卷 / 04期
关键词
acharan sulfate; Achatina fulica; glycosaminoglycans; mucus; organic shell matrix; snail;
D O I
10.1111/j.1432-1033.2004.03989.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Acharan sulfate, a recently discovered glycosaminoglycan isolated from Achatina fulica, has a major disaccharide repeating unit of -->4)-2-acetyl,2-deoxy-alpha-D-glucopyranose(1-->4)-2-sulfo-alpha-L-idopyranosyluronic acid (1-->, making it structurally related to both heparin and heparan sulfate. It has been suggested that this glycosaminoglycan is polydisperse, with an average molecular mass of 29 kDa and known minor disaccharide sequence variants containing unsulfated iduronic acid. Acharan sulfate was found to be located in the body of this species using alcian blue staining and it was suggested to be the main constituent of the mucus. In the present work, we provide further information on the structure and compartmental distribution of acharan sulfate in the snail body. Different populations of acharan sulfate presenting charge and/or molecular mass heterogeneities were isolated from the whole body, as well as from mucus and from the organic shell matrix. A minor glycosaminoglycan fraction susceptible to degradation by nitrous acid was also purified from the snail body, suggesting the presence of N-sulfated glycosaminoglycan molecules. In addition, we demonstrate the in vivo metabolic labeling of acharan sulfate in the snail body after a meal supplemented with [S-35]free sulfate. This simple approach might be applied to the study of acharan sulfate biosynthesis. Finally, we developed histochemical assays to localize acharan sulfate in the snail body by metachromatic staining and by histoautoradiography following metabolic radiolabeling with [S-35]sulfate. Our results show that acharan sulfate is widely distributed among several organs.
引用
收藏
页码:845 / 854
页数:10
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