Novel fluorescence biosensor custom-made for protein tyrosine phosphatase 1B detection based on titanium dioxide-decorated single-walled carbon nanohorn nanocomposite

被引:7
作者
Feng, Tingting [1 ]
Yan, Shuzhu [1 ]
Hou, Shanshan [3 ]
Fan, Xiaohui [2 ]
机构
[1] Shanxi Univ Chinese Med, Coll Tradit Chinese Med & Food Engn, Jinzhong 030619, Peoples R China
[2] Zhejiang Univ, Pharmaceut Informat Inst, Coll Pharmaceut Sci, Hangzhou 310058, Peoples R China
[3] Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Liaoning, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
TiO; 2-SWCNHs; Fluorescent; PTP1B; Phosphopeptide; Biosensor; SENSITIVE DETECTION; ASSAY;
D O I
10.1016/j.saa.2022.121548
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
This paper presents a new fluorescent approach for the detection of protein tyrosine phosphatase 1B (PTP1B) based on titanium dioxide-decorated single-wall carbon nanohorns (TiO2-SWCNHs). The novel TiO2-SWCNHs nanocomposite was synthesized and characterized for the first time and the phosphorylated peptide as the substrate of PTP1B was designed. Properties of SWCNHs and TiO2 were combined by growing nano-sized TiO2 particles on SWCNHs, resulting in TiO2-SWCNHs. TiO2 provides SWCNHs a large adsorption surface area and can specifically bind to phosphopeptide substrate. TiO2-SWCNHs effectively quenched the fluorescence of the phosphorylated peptide substrate labeled by the fluorophore, and the system had a low fluorescence background. In the presence of PTP1B, dephosphorylation of the peptide occurred owing to the reaction between PTP1B and the peptide, causing the separation of the dye-labeled peptide from TiO2-SWCNHs, which resulted in fluorescence enhancement of the reaction system. Thus, a simple and rapid strategy for the detection of PTP1B activity was developed, with a detection limit of 0.01 ng/mL and linear range of 0-10 ng/mL. The system can be used to detect PTP1B in serum using the standard addition method. This system provides a new approach for screening PTP1B inhibitors.
引用
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页数:8
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