Immobilization of aptamer-modified gold nanoparticles on BiOCl nanosheets: Tunable peroxidase-like activity by protein recognition

被引:54
作者
Hsu, Chia-Lun [1 ]
Lien, Chia-Wen [1 ]
Wang, Chia-Wei [1 ]
Harroun, Scott G. [1 ]
Huang, Chih-Ching [2 ,3 ,4 ]
Chang, Huan-Tsung [1 ]
机构
[1] Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan
[2] Natl Taiwan Ocean Univ, Dept Biosci & Biotechnol, Keelung 20224, Taiwan
[3] Natl Taiwan Ocean Univ, Ctr Excellence Oceans, Keelung 20224, Taiwan
[4] Kaohsiung Med Univ, Coll Pharm, Sch Pharm, Kaohsiung 80708, Taiwan
关键词
Enzyme; Self-assembly; Nanoparticles; Aptamers; Synergistic effects; DISPERSED CARBON NANOTUBES; ENDOTHELIAL GROWTH-FACTOR; ENZYME-LIKE ACTIVITY; GRAPHENE OXIDE; CATALYTIC-ACTIVITY; 001; FACETS; NANOMATERIALS; IMPROVEMENT; OXIDATION; MIMICS;
D O I
10.1016/j.bios.2015.08.049
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A self-assembled nanocomposite is prepared from an aqueous mixture of aptamer-modified gold nanoparticles (Apt-Au NPs), bismuth ions and chloride ions. The Apt-Au NPs are immobilized on bismuth oxychloride (BiOCl) nanosheets in situ to form Apt-Au NPs/BiOCl nanocomposites. The as-prepared nanocomposites exhibit high peroxidase-like activity for the catalytic conversion of Amplest Red (AR) to fluorescent resorufin in the presence of H2O2. The catalytic activity of Apt-Au NPs/BiOCl nanocomposites is at least 90-fold higher than that of Apt-Au NPs or BiOCl nanosheets, revealing synergistic effects on their activity. The catalytic activity of Apt-Au NPs/BiOCl nanocomposites is suppressed by vascular endothelial growth factor-A(165) (VEGF-A(165)) molecules that specifically interact with the aptamer units (Del-5-1 and v7t-1) on the nanocomposite surface. The AR/H2O2-Apt-Au NPs/BiOCl nanocomposites probe shows high selectivity (> 1000-fold over other proteins) and sensitivity (detection limit similar to 0.5 nM) for the detection of VEGF-A(165). Furthermore, the probe is employed for the detection of VEGF isoforms and for the study of interactions between VEGF and VEGF receptors. The practicality of this simple, rapid, cost-effective probe is validated by the analysis of VEGF-A(165) in cell culture media, showing its great potential for the analysis of VEGF in biological samples. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:181 / 187
页数:7
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