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.
引用
收藏
页码:2637 / 2644
页数:8
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