Preparation of lectin-vicilin nanoparticle conjugates using the carbodiimide coupling technique

被引:25
作者
Ezpeleta, I
Irache, JM
Stainmesse, S
Chabenat, C
Gueguen, J
Orecchioni, AM
机构
[1] UNIV ROUEN, DEPT PHARM GALEN, LAB PHARMACOCHIM & BIOPHARM, EA DRED 1295, F-76803 ST ETIENNE DU ROUVRAY, FRANCE
[2] UNIV ROUEN, DEPT CHIM ANALYT, F-76803 ST ETIENNE DU ROUVRAY, FRANCE
[3] INRA, BIOCHIM & TECHNOL PROT LAB, F-44026 NANTES, FRANCE
关键词
vicilin; nanoparticles; lectin; mucin; conjugates; carbodiimide;
D O I
10.1016/0378-5173(96)04668-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This work describes the preparation and the in vitro activity of conjugates formed by Ulex europaeus lectin (UE lectin) and vicilin (storage protein from Pisum sativum) nanoparticles. The lectin was fixed by coupling its amino groups to carbodiimide-activated carboxylic groups on the vicilin nanoparticles. The influence of the carbodiimide concentration and the reaction time was studied. Typically, the amount of bound lectin was calculated to be about 30 mu g lectin/mg nanoparticles, which corresponded to a lectin coupling efficiency of about 21%. Furthermore, the activity and the specificity of these conjugates was tested with bovine submaxillary gland mucin (BSM), When the experiences were carried out in the absence of L-fucose (specific sugar for UE lectin), the UE lectin-vicilin nanoparticle conjugates showed three times more interaction with mucin than the control (vicilin nanoparticles). Moreover, the specificity of the lectin was maintained after coupling to vicilin nanoparticles because the presence of L-fucose inhibited the interactions between conjugates and mucin.
引用
收藏
页码:227 / 233
页数:7
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