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
相关论文
共 35 条
[1]   The role of hydrophobic side chains as determinants of antibacterial activity of semisynthetic glycopeptide antibiotics [J].
Allen, NE ;
LeTourneau, DL ;
Hobbs, JN .
JOURNAL OF ANTIBIOTICS, 1997, 50 (08) :677-684
[2]   Influence of anchor lipids on the homogeneity and mobility of lipid bilayers on thin polymer films [J].
Beyer, D ;
Elender, G ;
Knoll, W ;
Kuhner, M ;
Maus, S ;
Ringsdorf, H ;
Sackmann, E .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1996, 35 (15) :1682-1685
[3]  
Burden R. L., 2011, NUMERICAL ANAL, V9th
[4]   Kinetic analysis of antibody-antigen interactions at a supported lipid monolayer [J].
Cooper, MA ;
Williams, DH .
ANALYTICAL BIOCHEMISTRY, 1999, 276 (01) :36-47
[5]   Bacillus thuringiensis Cry1Ac toxin interaction with Manduca sexta aminopeptidase N in a model membrane environment [J].
Cooper, MA ;
Carroll, J ;
Travis, ER ;
Williams, DH ;
Ellar, DJ .
BIOCHEMICAL JOURNAL, 1998, 333 :677-683
[6]   Surface plasmon resonance analysis at a supported lipid monolayer [J].
Cooper, MA ;
Try, AC ;
Carroll, J ;
Ellar, DJ ;
Williams, DH .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1998, 1373 (01) :101-111
[7]  
COOPER MA, 1997, J CHEM SOC CHEM COMM, P1625
[8]   INTERACTION OF VIBRIO-CHOLERAE ENTEROTOXIN WITH CELL-MEMBRANES [J].
CUATRECASAS, P .
BIOCHEMISTRY, 1973, 12 (18) :3547-3558
[9]   STRUCTURAL CHARACTERIZATION OF LANGMUIR-BLODGETT MULTILAYER ASSEMBLIES BY PLASMON SURFACE POLARITON FIELD-ENHANCED RAMAN-SPECTROSCOPY [J].
DUSCHL, C ;
KNOLL, W .
JOURNAL OF CHEMICAL PHYSICS, 1988, 88 (06) :4062-4069
[10]   19F NMR in the measurement of binding affinities of chloroeremomycin to model bacterial cell-wall surfaces that mimic VanA and VanB resistance [J].
Entress, RMH ;
Dancer, RJ ;
O'Brien, DP ;
Try, AC ;
Cooper, MA ;
Williams, DH .
CHEMISTRY & BIOLOGY, 1998, 5 (06) :329-337