Genetically functionalized ferritin nanoparticles with a high-affinity protein binder for immunoassay and imaging

被引:16
|
作者
Kim, Jong-Won [1 ]
Heu, Woosung [2 ]
Jeong, Sukyo [2 ]
Kim, Hak-Sung [2 ]
机构
[1] Korea Adv Inst Sci & Technol, Grad Sch Nanosci & Technol, Daejeon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Biol Sci, Daejeon 305701, South Korea
基金
新加坡国家研究基金会;
关键词
Repebody; Ferritin; Self-assembly; Multivalency; Immunoassay; Cell imaging; CARBOHYDRATE ANTIGEN 125; SIGNAL AMPLIFICATION; DRUG-DELIVERY; ELECTROCHEMICAL IMMUNOASSAY; TUMOR-CELLS; H-CHAIN; BINDING; APOFERRITIN; CANCER; EXPRESSION;
D O I
10.1016/j.aca.2017.07.060
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Molecular detection of target molecules with high sensitivity and specificity is of great significance in bio and medical sciences. Here, we present genetically functionalized ferritin nanoparticles with a high-affinity protein binder, and their utility as a signal generator in a variety of immunoassays and imaging. As a high-affinity protein binder, human IgG-specific repebody, which is composed of LRR (Leucinerich repeat) modules, was used. The repebody was genetically fused to the N-terminal heavy-chain ferritin, and the resulting subunits were self-assembled to the repebody-ferritin nanoparticles composed of 24 subunits. The repebody-ferritin nanoparticles were shown to have a three-order of magnitude higher binding affinity toward human IgG than free repebody mainly owing to a decreased dissociation rate constant. The repebody-ferritin nanoparticles were conjugated with fluorescent dyes, and the resulting nanoparticles were used for western blotting, cell imaging, and flow cytometric analysis. The dye-labeled repebody-ferritin nanoparticles were shown to generate about 3-fold stronger fluorescent signals in immunoassays than monovalent repebody. The repebody-functionalized ferritin nanoparticles can be effectively used for sensitive and specific immunoassays and imaging in many areas. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:81 / 88
页数:8
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