Recognition of bacterial lipopolysaccharide using bacteriophage-adhesin-coated long-period gratings

被引:64
作者
Brzozowska, Ewa [1 ]
Smietana, Mateusz [2 ]
Koba, Marcin [3 ,4 ]
Gorska, Sabina [1 ]
Pawlik, Krzysztof [1 ]
Gamian, Andrzej [1 ]
Bock, Wojtek J. [4 ]
机构
[1] Polish Acad Sci, Inst Immunol & Expt Therapy, PL-53114 Wroclaw, Poland
[2] Warsaw Univ Technol, Inst Microelect & Optoelect, PL-00662 Warsaw, Poland
[3] Inst Natl Telecommun, PL-04894 Warsaw, Poland
[4] Univ Quebec Outaouais, Ctr Rech Photon, Gatineau, PQ J8X 3X7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Optical fiber sensors; Long-period gratings (LPG); Label-free sensing; Biosensors; Bacterial lipopolysaccharide (LPS); Bacteriophage adhesin; FIBER GRATINGS; T4; TAIL; PROTEINS; MORPHOGENESIS; SENSITIVITY; ENDOTOXIN;
D O I
10.1016/j.bios.2014.07.027
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this paper we present a new type of highly sensitive label-free sensor based on long-period gratings (LPG) coated with T4 bacteriophage (phage) adhesin. The adhesin (gp37) binds Escherichia coli B (E. coli B) by recognizing its bacterial lipopolysaccharide (LPS). The LPG biofunctionalization methodology is based on coating LPG surface with nickel ions capable of gp37 histidine tag reversible binding. For the first time recombinant adhesive phage protein has been used as a receptor molecule in biosensing scheme. The specificity of LPS binding by adhesin has been tested with LPG-based device and confirmed using Western blot, Enzyme-Linked Immunosorbent Assay (ELISA) and BIACORE methods. The LPG-based sensor can measure bacterial contamination in real time and with a high accuracy. We show that T4 phage adhesin binds E. coli B LPS in its native or denatured form. The binding is highly specific and irreversible. The applied procedure allows for obtaining reusable biosensors. (C) 2014 Elsevier ay. All rights reserved.
引用
收藏
页码:93 / 99
页数:7
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