A novel arginine bioprobe based on up-conversion fluorescence resonance energy transfer

被引:19
作者
Wu, Jiasheng [1 ]
Wang, Hao [2 ]
Yang, Hao [1 ]
Chen, Jing [1 ]
Yang, Haipeng [1 ]
机构
[1] Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen Key Lab Polymer Sci & Technol, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Coll Mech & Control Engn, Guangdong Prov Key Lab Micro Nano Optomechatron E, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
NaYF4; Fluorescence resonance energy transfer; Arginine; Bioprobe; Up-conversion phosphor; QUANTUM DOTS; HYDROTHERMAL SYNTHESIS; GOLD NANOPARTICLES; ASSAY; DONOR; NAYF4YB3+; BIOSENSOR; SENSOR; FRET;
D O I
10.1016/j.aca.2019.06.060
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Arginine is an important amino acid in humankind bodies and is of essential clinical significance. This paper presents a novel bioprobe based on fluorescence resonance energy transfer (FRET), which can be used to detect arginine efficiently and economically. In this bioprobe system, positively charged upconversion phosphor NaYF4 (NYF) acts as energy donor, and negatively charged gold nanoparticle (AuNP) acts as energy acceptor. The oppositely charged donor and acceptor come into close proximity through electrostatic attraction effect, which results in the occurrence of FRET between NYF and AuNP. The FRET process is thus in the "on" state, meanwhile the system is in the "off" state, and the emitting light of NYF quenched. When positively charged arginine is added into the system, the guanidyl of arginine binds to AuNP and leads to the negatively charged AuNP becomes positively charged one, and the AuNP separates from NYF because of the electrostatic repulsion. The FRET process is blocked and the system switches to the "on" state because the distance between NYF and AuNP becomes longer. In the "on" state, the intensity of the restored emitting light is proportional to the concentration of arginine. This approach brings a good linear relationship between the fluorescence intensity and the concentration of arginine in the concentration range of 14.42-115.04 mu M. The limit of detection is as low as 2.9 mu M. A new method for quantitative determination of arginine by just measuring the fluorescence intensity of the system is established. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:200 / 206
页数:7
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