Using biofunctionalized nanoparticles to probe pathogenic bacteria

被引:126
作者
Ho, KC
Tsai, PJ
Lin, YS
Chen, YC [1 ]
机构
[1] Natl Chiao Tung Univ, Dept Appl Chem, Hsinchu 300, Taiwan
[2] Tzu Chi Univ, Dept Lab Med & Biotechnol, Hualien 970, Taiwan
关键词
D O I
10.1021/ac048688b
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this paper, we report a method for fabricating biofunctionalized nanoparticles by attaching human immunoglobulin (IgG) onto their surfaces through either electrostatic interactions or covalent binding. We found that these IgG-presenting nanoparticles can bind selectively to the cell walls of pathogens that contain IgG-binding sites based on the investigation of transmission electron microscopy images. Our results demonstrate that such Au-IgG nanoparticles may serve as useful nanoscale probes for exploring the interactions between IgG and pathogens. Furthermore, the IgG-presenting magnetic nanoparticles have been employed as effective affinity probes for selectively concentrating traces of target bacteria from sample solutions. The trapped bacteria were then characterized by using matrix-assisted laser desorption/ionization mass spectrometry. The lowest cell concentration we detected for both Staphylococcus saprophyticus and Staphylococcus aureus in aqueous sample solutions (0.5 mL) was similar to3 x 10(5) cfu/mL, while the detectable cell concentration for S. saprophyticus in a urine sample was similar to3 x 10(7) cfu/mL.
引用
收藏
页码:7162 / 7168
页数:7
相关论文
共 38 条
[1]   Electrostatic layer-by-layer nanoassembly on biological microtemplates: Platelets [J].
Ai, H ;
Fang, M ;
Jones, SA ;
Lvov, YM .
BIOMACROMOLECULES, 2002, 3 (03) :560-564
[2]   ROUTINE DIAGNOSTIC TEST FOR IGA AND IGM ANTIBODIES TO RUBELLA-VIRUS - ABSORPTION OF IGG WITH STAPHYLOCOCCUS-AUREUS [J].
ANKERST, J ;
CHRISTENSEN, P ;
KJELLEN, L ;
KRONVALL, G .
JOURNAL OF INFECTIOUS DISEASES, 1974, 130 (03) :268-273
[3]  
Arnold RJ, 1998, RAPID COMMUN MASS SP, V12, P630, DOI 10.1002/(SICI)1097-0231(19980529)12:10<630::AID-RCM206>3.3.CO
[4]  
2-S
[5]   Opsonic human antibodies from an endemic population specific for a conserved epitope on the M protein of group A streptococci [J].
Brandt, ER ;
Hayman, WA ;
Currie, B ;
Carapetis, J ;
Wood, Y ;
Jackson, DC ;
Cooper, J ;
Melrose, WD ;
Saul, AJ ;
Good, MF .
IMMUNOLOGY, 1996, 89 (03) :331-337
[6]   RAPID IMMUNOFLUORESCENT PROCEDURE FOR DETECTION OF SPECIFIC IGG AND IGM ANTIBODY IN SERA USING STAPHYLOCOCCUS-AUREUS AND LATEX-IGG AS ABSORBENTS [J].
CHANTLER, S ;
DEVRIES, E ;
ALLEN, PR ;
HURN, BAL .
JOURNAL OF IMMUNOLOGICAL METHODS, 1976, 13 (3-4) :367-380
[7]   The rapid identification of intact microorganisms using mass spectrometry [J].
Claydon, MA ;
Davey, SN ;
EdwardsJones, V ;
Gordon, DB .
NATURE BIOTECHNOLOGY, 1996, 14 (11) :1584-1586
[8]  
Dai YQ, 1999, RAPID COMMUN MASS SP, V13, P73
[9]   Microorganism identification by mass spectrometry and protein database searches [J].
Demirev, PA ;
Ho, YP ;
Ryzhov, V ;
Fenselau, C .
ANALYTICAL CHEMISTRY, 1999, 71 (14) :2732-2738
[10]   Monitoring protein expression in whole bacterial cells with MALDI time-of-flight mass spectrometry [J].
Easterling, ML ;
Colangelo, CM ;
Scott, RA ;
Amster, IJ .
ANALYTICAL CHEMISTRY, 1998, 70 (13) :2704-2709