A vesicle capture sensor chip for kinetic analysis of interactions with membrane-bound receptors

被引:151
作者
Cooper, MA
Hansson, A
Löfås, S
Williams, DH
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[2] Biacore AB, SE-75450 Uppsala, Sweden
基金
英国生物技术与生命科学研究理事会;
关键词
surface plasmon resonance; liposome; glycopeptide antibiotic; cholera toxin; DNA hybridization;
D O I
10.1006/abio.1999.4389
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel sensor chip for use in surface plasmon resonance (SPR) biosensors has been developed to capture vesicles which may contain membrane-bound receptors, Sulforhodamine-containing vesicles were shown by fluorescence microscopy to be immobilized intact on the sensor chip. Binding of cholera toxin to captured vesicles containing ganglioside GM, was demonstrated using SPR, and the derived kinetic and affinity constants were similar to literature values. Biotinylated vesicles captured on the sensor chip were used to bind streptavidin and then biotinylated ss-DNA The hybridization of complementary ss-DNA to the immobilized ss-DNA was then analyzed using SPR, The values obtained were similar to those obtained for an identical interaction analyzed using a commercially available streptavidin-containing sensor chip. Binding of vancomycin-group antibiotics to captured vesicles containing a bacterial cell wall mucopeptide analogue was demonstrated. No binding of the bacterial endotoxin Cry1A(c) to captured vesicles containing its cell surface receptor could be demonstrated, (C) 2000 Academic Press.
引用
收藏
页码:196 / 205
页数:10
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