Graying the self-assembly of gold nanoparticles for improved enzyme activity assays

被引:7
作者
Kim, Gae Bails [1 ,2 ]
Lee, Jin Oh [1 ,2 ]
Kim, Young-Pil [1 ,2 ,3 ]
机构
[1] Hanyang Univ, Dept Life Sci, Seoul 04763, South Korea
[2] Hanyang Univ, Res Inst Nat Sci, Seoul 04763, South Korea
[3] Hanyang Univ, Inst Nano Sci & Technol, Seoul 04763, South Korea
来源
SENSORS AND ACTUATORS B-CHEMICAL | 2017年 / 246卷
基金
新加坡国家研究基金会;
关键词
Gold nanoparticle; Silver enhancement; Signal amplification; Self-assembly; Enzyme activity; ENHANCED RAMAN-SPECTROSCOPY; SILVER ENHANCEMENT; COLORIMETRIC DETECTION; AGGREGATION; IMMUNOASSAY; NANOSENSORS; SENSORS; DNA;
D O I
10.1016/j.snb.2017.02.067
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Despite the simplicity and usability of gold nanoparticle (AuNP)-based colorimetry in a large panel of bioassays, this technique still suffers from a poor detection limit. To overcome this issue, we report an improved AuNP-based colorimetric assay in combination with simple centrifugation and silver enhancement. As a proof-of-concept, two types of enzymes (i.e., protein phosphatase and protease) were constructed based on the self-assembly of thiol-stabilized AuNPs in the presence of peptides and metal ions. When the AuNP solutions were subjected to a short cycle of centrifugation and silver enhancement, the signal-to-background ratio (SBR) was distinctly improved by a factor of 5-10 in both enzyme activity assays, as compared to that of AuNP-based colorimetry. The detection limit achieved by using the silver enhancement was determined to be improved by a factor of 1.0-3.4. Furthermore, grayscale images of the silver enhancement allowed for a rapid andsimple enzyme assay that did not require measuring.the absorbance. Due to its ability to improve the detection senstivity in a facile way, we anticipate that this approach will be suitable for use in many AuNP colorimetric assays. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:271 / 277
页数:7
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