Preparation and evaluation of spore-specific affinity-augmented bio-imprinted beads

被引:31
作者
Harvey, Scott D. [1 ]
Mong, Gary M. [1 ]
Ozanich, Richard M. [1 ]
Mclean, Jeffrey S. [1 ]
Goodwin, Shannon M. [1 ]
Valentine, Nancy B. [1 ]
Fredrickson, Jim K. [1 ]
机构
[1] Pacific NW Natl Lab, Richland, WA 99352 USA
关键词
bio-imprinted beads; selective spore capture/concentration; analysis of biological pathogens;
D O I
10.1007/s00216-006-0622-z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel, affinity-augmented, bacterial spore-imprinted, bead material was synthesized, based on a procedure developed for vegetative bacteria. The imprinted beads were intended as a front-end spore capture/concentration stage of an integrated biological detection system. Our approach involved embedding bead surfaces with Bacillus thuringiensis kurstaki (Bt) spores (as a surrogate for Bacillus anthracis) during synthesis. Subsequent steps involved lithographic deactivation using a perfluoroether; spore removal to create imprint sites; and coating imprints with the lectin, concanavalin A, to provide general affinity. The synthesis of the intended material with the desired imprints was verified by scanning electron and confocal laser-scanning microscopy. The material was evaluated using spore-binding assays with either Bt or Bacillus subtilis (Bs) spores. The binding assays indicated strong spore-binding capability and a robust imprinting effect that accounted for 25% additional binding over non-imprinted controls. The binding assay results also indicated that further refinement of the surface deactivation procedure would enhance the performance of the imprinted substrate.
引用
收藏
页码:211 / 219
页数:9
相关论文
共 26 条
[1]   Bacteria-mediated lithography of polymer surfaces [J].
Aherne, A ;
Alexander, C ;
Payne, MJ ;
Perez, N ;
Vulfson, EN .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (36) :8771-8772
[2]   Spatially functionalized polymer surfaces produced via cell-mediated lithography [J].
Alexander, C ;
Vulfson, EN .
ADVANCED MATERIALS, 1997, 9 (09) :751-755
[3]  
Alexander C, 2004, POLYM CHEM PRACTICAL, P201
[4]  
AMRSHALL KC, 1991, MICROBIAL CELL SURFA, P5
[5]  
[Anonymous], 1990, Molecular biological methods for Bacillus, DOI DOI 10.1111/J.1751-1097.1991.TB02087.X
[6]  
Berry ED, 1999, J RAPID METH AUT MIC, V7, P7
[7]   Renewable microcolumns for automated DNA purification and flow-through amplification: from sediment samples through polymerase chain reaction [J].
Bruckner-Lea, CJ ;
Tsukuda, T ;
Dockendorff, B ;
Follansbee, JC ;
Kingsley, MT ;
Ocampo, C ;
Stults, JR ;
Chandler, DP .
ANALYTICA CHIMICA ACTA, 2002, 469 (01) :129-140
[8]   Lectin-based affinity capture for MALDI-MS analysis of bacteria [J].
Bundy, J ;
Fenselau, C .
ANALYTICAL CHEMISTRY, 1999, 71 (07) :1460-1463
[9]   Lectin and carbohydrate affinity capture surfaces for mass spectrometric analysis of microorganisms [J].
Bundy, JL ;
Fenselau, C .
ANALYTICAL CHEMISTRY, 2001, 73 (04) :751-757
[10]   Automated immunomagnetic separation and microarray detection of E-coli O157:H7 from poultry carcass rinse [J].
Chandler, DP ;
Brown, J ;
Call, DR ;
Wunschel, S ;
Grate, JW ;
Holman, DA ;
Olson, L ;
Stottlemyre, MS ;
Bruckner-Lea, CJ .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2001, 70 (1-2) :143-154