Immobilization of biotinylated bacteriophages on biosensor surfaces

被引:96
作者
Gervals, L.
Gel, M.
Allain, B.
Tolba, M.
Brovko, L.
Zourob, M.
Mandeville, R.
Griffiths, M.
Evoy, S. [1 ]
机构
[1] Univ Alberta, Dept Elect & Comp Engn, Edmonton, AB T6G 2V4, Canada
[2] Univ Alberta, Natl Inst Nanoteechnol, Edmonton, AB T6G 2V4, Canada
[3] Biophage Pharm Inc, Montreal, PQ H4P 2R2, Canada
[4] Univ Guelph, Canadian Res Inst Food Safety, Guelph, ON N1G 2W1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
bacteriophage; biosensor; bacteria; impedance sensing; biotinylation;
D O I
10.1016/j.snb.2007.03.007
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Bacteriophages are viruses that recognize specific receptors on the bacterium surface to which they bind and inject genetic material. The specificity of this recognition opens remarkable possibilities for biosensor development. The chemical attachment of T4 bacteriophages onto,gold surfaces is being reported. This attachment leverages the genetic biotinylation of the capsid heads of bacteriophages, and the natural affinity of the biotin/streptavidin system. The development of a streptavidin-immobilization chemistry that minimizes non-specific binding of the target bacterium is first described. The attachment of genetically biotinylated T4 bacteriophages onto these streptavidin-coated surfaces is then reported. Such chemical immobilization results in a 15-fold improvement of attachment when compared to the simple physisorption of the wild-type phage onto bare gold. The attachment procedure was then used to investigate the effect of a biotinylated phage-terminated surface on the growth of the host bacteria. This assessment was conducted in an electric cell-substrate impedance sensing device. The streptavidin-mediated attachment of biotinylated phages significantly delays the growth of the host bacteria by up to 17.2h. In comparison, non-specific binding of wild-type phages onto the streptavidin surface is found to cause a lesser growth delay of 13 h. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:615 / 621
页数:7
相关论文
共 28 条
[11]   Virus detection using nanoelectromechanical devices [J].
Ilic, B ;
Yang, Y ;
Craighead, HG .
APPLIED PHYSICS LETTERS, 2004, 85 (13) :2604-2606
[12]   Rapid detection of Salmonella enterica serovar choleraesuis in blood cultures by a dot blot enzyme-linked immunosorbent assay [J].
Janyapoon, K ;
Korbsrisate, S ;
Thamapa, H ;
Thongmin, S ;
Kanjanahareutai, S ;
Wongpredee, N ;
Sarasombath, S .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2000, 7 (06) :977-979
[13]  
Jia XE, 2006, CHINESE CHEM LETT, V17, P509
[14]   PCR-ELISA for the early diagnosis of invasive pulmonary aspergillus infection in neutropenic patients [J].
Jones, ME ;
Fox, AJ ;
Barnes, AJ ;
Oppenheim, BA ;
Balagopal, P ;
Morgenstern, GR ;
Scarffe, JH .
JOURNAL OF CLINICAL PATHOLOGY, 1998, 51 (09) :652-656
[15]   Antimicrobial peptides for detection of bacteria in biosensor assays [J].
Kulagina, NV ;
Lassman, ME ;
Ligler, FS ;
Taitt, CR .
ANALYTICAL CHEMISTRY, 2005, 77 (19) :6504-6508
[16]  
Kutter E., 2004, BACTERIOPHAGES BIOL, DOI [10.1201/9780203491751, DOI 10.1201/9780203491751]
[17]   Advances in biosensors for detection of pathogens in food and water [J].
Leonard, P ;
Hearty, S ;
Brennan, J ;
Dunne, L ;
Quinn, J ;
Chakraborty, T ;
O'Kennedy, R .
ENZYME AND MICROBIAL TECHNOLOGY, 2003, 32 (01) :3-13
[18]   Array biosensor for detection of toxins [J].
Ligler, FS ;
Taitt, CR ;
Shriver-Lake, LC ;
Sapsford, KE ;
Shubin, Y ;
Golden, JP .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2003, 377 (03) :469-477
[19]   Multiplex PCR assay for detection of bacterial pathogens associated with warm-water streptococcosis in fish [J].
Mata, AI ;
Gibello, A ;
Casamayor, A ;
Blanco, MM ;
Domínguez, L ;
Fernández-Garayzábal, JF .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (05) :3183-3187
[20]   A PCR assay for detection of acetic acid-tolerant lactic acid bacteria in acidic food products [J].
Nakano, S ;
Matsumura, A ;
Yamada, T .
JOURNAL OF FOOD PROTECTION, 2004, 67 (03) :610-615