Ultrasensitive electrochemical biosensor for microRNA-377 detection based on MXene-Au nanocomposite and G-quadruplex nano-amplification strategy

被引:35
作者
Wu, Qianqing [1 ,2 ]
Li, Zhenhui [3 ]
Liang, Qianwei [2 ]
Ye, Rongkai [2 ]
Guo, Shuzhou [2 ]
Zeng, Xiaobing [2 ]
Hu, Jianqiang [2 ]
Li, Aiqing [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Guangdong Prov Inst Nephrol, Natl Clin Res Ctr Kidney Dis,State Key Lab Organ F, Guangzhou 510515, Peoples R China
[2] South China Univ Technol, Sch Chem & Chem Engn, Key Lab Fuel Cell Technol Guangdong Prov, Guangzhou 510641, Peoples R China
[3] Shishi Gen Hosp, Dept Nephrol, Quanzhou 362700, Shishi, Peoples R China
关键词
MXene; Au nanocomposites; G-quadruplex; MicroRNA-377; Electrochemical biosensor; Nano; -amplification; NANOMATERIALS; BIOMARKERS; TARGET; CANCER; H2O2;
D O I
10.1016/j.electacta.2022.140945
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
MicroRNAs (miRNAs) are considered as potential biomarkers for early diagnosis and prognostic assessment of diabetic nephropathy. In this work, an electrochemical biosensor for ultrasensitive detection of miRNA-377 was constructed based on MXene-Au nanocomposites and G-quadruplex nano-amplification strategy. As a promising nanocarrier, taking advantage of leveraging synergistic effects between Au nanoparticles (AuNPs) and MXene nanosheet, MXene-Au nanocomposites exhibited excellent electronic conductivity and provided massive active sites for DNA capture probe immobilization by Au-S bonds. AuNPs modified with Guanine-rich sequence DNA detection probes were designed as signal amplification nano-labels. Specifically, by inducing the transition of Guanine-rich detection probes to G-quadruplex, the strong affinity interaction between methylene blue and G-quadruplex could not only reflect trace concentration information of miRNA-377, but also lead to the further enhancement of electrochemical signal (2.7-fold). As a result, this newly designed biosensor exhibited superior sensing performance with a wide linear range from 10 aM to 100 pM and the limit of detection was as low as 1.35 aM. Compared with biosensors based on other nanocomposites and reported miRNA-377 biosensors, the pro-posed sensing platform did not require any thermal cycling or reverse transcription process, meeting the miRNA sensing requirements of convenient, sensitive, specific and stable. Furthermore, the as-constructed biosensor also displayed good selectivity, which was applied to accurate detection of miRNA-377 in human serum samples with satisfactory sensitivity, suggesting the biosensor system has promising applications in biological researches and early clinical diagnosis for diabetic nephropathy.
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页数:8
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