Hybridization-triggered isothermal signal amplification coupled with MutS for label-free and sensitive fluorescent assay of SNPs

被引:16
作者
Jiao, Anli [1 ,2 ]
Zheng, Jing [1 ,2 ,3 ,4 ,5 ]
Hu, Yaping [1 ,2 ]
Zhu, Guizhi [3 ,4 ,5 ]
Li, Jishan [1 ,2 ]
Li, Huimin [1 ,2 ]
Yang, Ronghua [1 ,2 ]
Tan, Weihong [1 ,2 ,3 ,4 ,5 ]
机构
[1] Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China
[2] Hunan Univ, Coll Mat & Engn, Changsha 410082, Hunan, Peoples R China
[3] Univ Florida, Ctr Res Bio Nano Interface, Dept Chem, Gainesville, FL 32611 USA
[4] Univ Florida, Dept Physiol & Funct Genom, Shands Canc Ctr, Gainesville, FL 32611 USA
[5] Univ Florida, UF Genet Inst, Gainesville, FL 32611 USA
关键词
SINGLE-NUCLEOTIDE POLYMORPHISMS; MOLECULAR BEACONS; DNA; STRAND; ELECTROPHORESIS; OLIGONUCLEOTIDE; COMPLEMENTARY; PROBES;
D O I
10.1039/c2cc30882g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Combining the specific recognization of MutS protein for mismatched DNA sequences with the target-driven molecular switch that acts as both the template and primer of the polymerization reaction, a new label-free and sensitive fluorescent assay strategy for specific single-stranded DNA sequences or SNPs is proposed.
引用
收藏
页码:5659 / 5661
页数:3
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