Multiple detection of single nucleotide polymorphism by microarray-based resonance light scattering assay with enlarged gold nanoparticle probes

被引:14
|
作者
Gao, Jiaxue [1 ,2 ]
Ma, Lan [1 ,3 ]
Lei, Zhen [1 ,2 ]
Wang, Zhenxin [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
[3] Ningxia Univ, Anal & Testing Ctr, Yinchuan 750021, Peoples R China
基金
中国国家自然科学基金;
关键词
ROLLING CIRCLE AMPLIFICATION; LIGASE CHAIN-REACTION; AU NANOPARTICLES; NUCLEIC-ACIDS; SNP DETECTION; DNA DETECTION; HUMAN GENOME; GROWTH; BIOSENSORS; PROTEINS;
D O I
10.1039/c5an02510a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The mapping of specific single nucleotide polymorphisms (SNPs) in patients' genome is a critical process for the development of personalized therapy. In this work, a DNA microarray-based resonance light scattering (RLS) assay has been developed for multiplexed detection of breast cancer related SNPs with high sensitivity and selectivity. After hybridization of the desired target single-stranded DNAs (ssDNAs) with the ssDNA probes on a microarray, the polyvalent ssDNA modified 13 nm gold nanoparticles (GNPs) are employed to label the hybridization reaction through the formation of a three-stranded DNA system. The H2O2-mediated enlargement of GNPs is then used to enhance the RLS signal. The microarray-based RLS assay provides a detection limit of 10 pM (S/N = 3) for the target ssDNA and determines an allele frequency as low as 1.0% in the target ssDNA cocktail. Combined with an asymmetric PCR technique, the proposed assay shows good accuracy and sensitivity in profiling 4 SNPs related to breast cancer of three selected cell lines.
引用
收藏
页码:1772 / 1778
页数:7
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