A biosensor based on electroactive dipyrromethene-Cu(II) layer deposited onto gold electrodes for the detection of antibodies against avian influenza virus type H5N1 in hen sera

被引:15
作者
Jarocka, Urszula [1 ]
Sawicka, Roza [2 ]
Stachyra, Anna [2 ]
Gora-Sochacka, Anna [2 ]
Sirko, Agnieszka [2 ]
Zagorski-Ostoja, Wlodzimierz [2 ]
Saczynska, Violetta [3 ]
Porebska, Anna [3 ]
Dehaen, Wim [4 ]
Radecki, Jerzy [1 ]
Radecka, Hanna [1 ]
机构
[1] Polish Acad Sci, Inst Anim Reprod & Food Res, PL-10748 Olsztyn, Poland
[2] Polish Acad Sci, Inst Biochem & Biophys, PL-02106 Warsaw, Poland
[3] Inst Biotechnol & Antibiot, PL-02516 Warsaw, Poland
[4] Univ Leuven, Dept Chem, B-3001 Leuven, Belgium
关键词
Dipyrromethene-Cu(II) layer; Histidine-tagged antigen immobilization; Detection of antibodies in sera; Avian influenza virus; SURFACE-PLASMON RESONANCE; ORIENTED IMMOBILIZATION; IMMUNOGLOBULIN-G; IMMUNOSENSOR; MONOLAYER; DOMAINS; BINDING; SENSOR;
D O I
10.1007/s00216-015-8949-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This paper describes the development of a biosensor for the detection of anti-hemagglutinin antibodies against the influenza virus hemagglutinin. The steps of biosensor fabrications are as follows: (i) creation of a mixed layer containing the thiol derivative of dipyrromethene and 4-mercapto-1-butanol, (ii) complexation of Cu(II) ions, (iii) oriented immobilization of the recombinant histidine-tagged hemagglutinin, and (iv) filling free spaces with bovine serum albumin. The interactions between recombinants hemagglutinin from the highly pathogenic avian influenza virus type H5N1 and anti-hemagglutinin H5 monoclonal antibodies were explored with Osteryoung square-wave voltammetry. The biosensor displayed a good detection limit of 2.4 pg/mL, quantification limit of 7.2 pg/mL, and dynamic range from 4.0 to 100.0 pg/mL in buffer. In addition, this analytical device was applied for the detection of antibodies in hen sera from individuals vaccinated and non-vaccinated against the avian influenza virus type H5N1. The limit of detection for the assay was the dilution of sera 1: 7 x 10(6), which is about 200 times better than the enzyme-linked immunosorbent assay.
引用
收藏
页码:7807 / 7814
页数:8
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