| Literature DB >> 26431499 |
Dong Men1,2, Ting-Ting Zhang2, Li-Wei Hou3, Juan Zhou1, Zhi-Ping Zhang1, Yuan-Yuan Shi4, Jin-Li Zhang5, Zong-Qiang Cui1, Jiao-Yu Deng1, Dian-Bing Wang6, Xian-En Zhang6.
Abstract
The self-assembly of nanoparticles into larger superstructures is a powerful strategy to develop novel functional nanomaterials, as these superstructures display collective properties that are different to those displayed by individual nanoparticles or bulk samples. However, there are increasing bottlenecks in terms of size control and multifunctionalization of nanoparticle assemblies. In this study, we developed a self-assembly strategy for construction of multifunctional nanoparticle assemblies of tunable size, through rational regulation of the number of self-assembling interaction sites on each nanoparticle. As proof-of-principle, a size-controlled enzyme nanocomposite (ENC) was constructed by self-assembly of streptavidin-labeled horseradish peroxidase (SA-HRP) and autobiotinylated ferritin nanoparticles (bFNP). Our ENC integrates a large number of enzyme molecules, together with a streptavidin-coated surface, allowing for a drastic increase in enzymatic signal when the SA is bound to a biotinylated target molecule. As result, a 10 000-fold increase in sensitivity over conventional enzyme-linked immunosorbent assays (ELISA) methods was achieved in a cardiac troponin immunoassay. Our method presented here should provide a feasible approach for constructing elaborate multifunctional superstructures of tunable size useful for a broad range of biomedical applications.Entities:
Keywords: enzyme nanocomposite; nanoparticles; self-assembly; ultrasensitive immunoassay
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Year: 2015 PMID: 26431499 DOI: 10.1021/acsnano.5b03607
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881