Catalytic ferromagnetic gold nanoparticle immunoassay for the detection and differentiation of Mycobacterium tuberculosis and Mycobacterium bovis

被引:9
作者
Gilbride, Brendan [1 ]
Moreira, Gustavo Marcal Schmidt Garcia [2 ]
Hust, Michael [2 ]
Cao, Cuong [1 ]
Stewart, Linda [1 ]
机构
[1] Queens Univ Belfast, Inst Global Food Secur, Sch Biol Sci, 19 Chlorine Gardens, Belfast BT9 5DL, Antrim, North Ireland
[2] Tech Univ Carolo Wilhelmina Braunschweig, Inst Biochem Biotechnol & Bioinformat, Abt Biotechnol, Braunschweig, Germany
关键词
Functionalised ferromagnetic gold nanoparticles; Peroxidase-mimic; Mycobacterium tuberculosis complex differentiation; Mycobacterium bovis; Immuno-biosensor; Monoclonal antibodies; ANTIGEN-DETECTION; DIAGNOSIS; ASSAY; IDENTIFICATION; EXPRESSION; UTILITY; MPT64; SIZE;
D O I
10.1016/j.aca.2021.339037
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A ferromagnetic gold nanoparticle based immune detection assay, exploiting the enhanced signal amplification of inorganic nanozymes, was developed and evaluated for its potential application in the detection of Mycobacterium tuberculosis complex (MTBC) organisms, and simultaneous identification of Mycobacterium bovis. Ferromagnetic gold nanoparticles (Au-Fe3O4 NPs) were prepared and their intrinsic peroxidase-like activity exploited to catalyse 3,30,5',5-tetramethylbenzidine (TMB) in the pres-ence of hydrogen peroxide (H2O2). When the Au-Fe3O4 NPs were functionalised by direct coupling with MTBC-selective antibodies, a nanoparticle based immune detection assay (NPIDA) was developed which could detect Mycobacterium tuberculosis (MTB) and differentiate M. bovis. In the assay, the intrinsic magnetic capability of the functionalised Au-Fe3O4 NPs was used in sample preparation to capture target bacterial cells. These were incorporated into a novel immunoassay which used species selective monoclonal antibodies (mAb) to detect bound target. The formation of a blue TMB oxidation product, with a peak absorbance of 370 nm, indicated successful capture and identification of the target. The detection limit of the NPIDA for both MTB and M. bovis was determined to be comparable to conventional ELISA using the same antibodies. Although limited matrix effects were observed in either assay, the NPIDA offers a reduced time to confirmatory identification. (C) 2021 Elsevier B.V. All rights reserved.
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页数:10
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