期刊
TALANTA
卷 167, 期 -, 页码 630-637出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.talanta.2017.03.001
关键词
SNP genotyping; DNAzyme sensor; Target-catalyzed hairpin assembly; Microfluidic; Chemiluminescence
资金
- National Science Foundation of China [21227007]
- Zhejiang Provincial Natural Science Foundation of China [LY16B050004]
- Interdisciplinary Seed Research Fund of Zhejiang University [JCZZ-2013010]
Single nucleotide polymorphisms (SNPs) are widely existed in human genome and associated with many diseases. Traditional PCR-based methods for SNP genotyping require protein enzyme, precise control of temperature and removal of resultant products, making the whole process labor intensive and time consuming. Although G-quadruplex DNAzyme-based assays provide many advantages over traditional approaches, the relatively low catalytic activity of DNAzyme becomes an unfavorable factor in its application process. Therefore, amplification of DNAzyme for further determination is of great desire in bioanalysis. In this work, we have developed an enzyme-free and non-label DNAzyme sensor for SNP genotyping based on target-catalyzed hairpin assembly (CHA) for DNAzyme amplification. The proposed sensor, carried out on microfluidic chemiluminescence (CL) assay, can sensitively discriminate rs242557 hotspot-SNP, the A/G single-nucleotide variation on human chromosome associated with Alzheimer's disease, with an absolute detection limit of 0.3 fmol.
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