An easy and sensitive sandwich assay for detection of Mycobacterium tuberculosis Ag85B antigen using quantum dots and gold nanorods

被引:52
作者
Kim, Eun Ju [1 ]
Kim, Eun Bee [1 ]
Lee, Seung Woo [1 ]
Cheon, Seon Ah [1 ]
Kim, Hwa-Jung [2 ,3 ]
Lee, Jaebeom [4 ]
Lee, Mi-Kyung [5 ]
Ko, Sungho [6 ]
Park, Tae Jung [1 ]
机构
[1] Chung Ang Univ, Dept Chem, 84 Heukseok Ro, Seoul 06974, South Korea
[2] Chungnam Natl Univ, Coll Med, Dept Microbiol, Daejeon 301747, South Korea
[3] Chungnam Natl Univ, Coll Med, Res Inst Med Sci, Daejeon 301747, South Korea
[4] Pusan Natl Univ, Dept Nano Fus & Cognomechatron Engn, Busan 609735, South Korea
[5] Chung Ang Univ Hosp, Dept Lab Med, 84 Heukseok Ro, Seoul 06974, South Korea
[6] CHA Univ, Dept Biotechnol, CHA Bio Complex,335 Pangyo Ro, Seongnam 463836, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
Mycobacterium tuberculosis; Ag85B; Biosensor; Gold nanorods; Quantum dots; ELECTRICAL DETECTION; BINDING POLYPEPTIDE; CDTE NANOCRYSTALS; ENERGY-TRANSFER; FRET ASSAY; SILICA; BIOSENSORS; SIZE; NANOPARTICLES; DIAGNOSIS;
D O I
10.1016/j.bios.2016.08.034
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Mycobacterium tuberculosis is a serious global infectious pathogen causing tuberculosis (TB). The development of an easy and sensitive method for the detection of M. tuberculosis is in urgent need due to complex and low specificity of the current assays. Herein, we present a novel method for M. tuberculosis detection based on a sandwich assay via antigen-antibody interaction using silica-coated quantum dots (SiQDs) and gold nanorods (AuNRs). A genetically engineered recombinant antibody (GBP-50B14 and SiBP-8B3) was bound to surfaces of AuNRs and SiQDs respectively, without any surface modification. The antigen-antibody interaction was revealed using M. tuberculosis-specific secretory antigen, Ag85B. Two biocomplexes showed a quenching effect in the presence of the target antigen through a sandwich assay. The assay response was in the range of 1 x 10(-3)-1 x 10(-10) mu g mL(-1) (R=0.969) and the limit of detection for Ag85B was 13.0 pg mL(-1). The Ag85B was selectively detected using three different proteins (CFP10, and BSA), and further specifically confirmed by the use of spiked samples. Compared with existing methods, a highly sensitive and selective method for Ag85B-expressing M. tuberculosis detection has been developed for better diagnosis of TB. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:150 / 156
页数:7
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