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Gold nanoparticle enhanced surface plasmon resonance imaging of microRNA-155 using a functional nucleic acid-based amplification machine
被引:39
|作者:
Zeng, Ke
[1
]
Li, Hongyuan
[2
]
Peng, Yinyin
[1
]
机构:
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Hematol, Chongqing 400016, Peoples R China
[2] Southwest Univ, Chongqing Key Lab Adv Mat & Technol Clean Energie, Chongqing 400715, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Biosensor;
Strand displacement amplification;
Hematological malignancies;
Gold nanoparticles;
Molecular beacon;
Enzymatic amplification;
Clinicalmolecular diagnostics;
Polydimethylsiloxane;
Gold island array microchips;
DNA hybridization;
LABEL-FREE;
SENSITIVE DETECTION;
HIGH-THROUGHPUT;
BIOSENSOR;
DNA;
STREPTAVIDIN;
PCR;
D O I:
10.1007/s00604-017-2276-2
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
MicroRNAs (miRNAs) are considered as being promising biomarkers for hematological malignancies, their aging, progression and prognosis. The authors have developed a method for the detection of miRNA155 by using surface plasmon resonance (SPR) imaging coupled to a nucleic acid-based amplification strategy using gold nanoparticles (AuNPs). The target miRNA155 is captured by surface-bound DNA probes. After hybridization, DNA-AuNP are employed for signal amplification via DNA sandwich assembly, resulting in a large increase in the SPR signal. This method can detect miRNA-155 in concentrations down to 45 pM and over dynamic that extends from 50 pM to 5 nM. The assay is highly specific and can discriminate even a single base mismatch. It also is reproducible, precise, and was successfully applied to the determination of miRNA-155 in spiked real samples where it gave recoveries in the range between 86% and 98%. This biosensor provides an alternative approach for miRNA detection in biomedical research and clinical diagnosis, which is highly effective and efficient.
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页码:2637 / 2644
页数:8
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