Amplification-by-Polymerization in Biosensing for Human Genomic DNA Detection

被引:18
作者
He, Peng [1 ,2 ]
Lou, Xinhui [2 ,3 ]
Woody, Susan M. [2 ,4 ]
He, Lin [2 ,5 ]
机构
[1] North Carolina Agr & Technol State Univ, Dept Chem, Greensboro, NC 27411 USA
[2] North Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
[3] Capital Normal Univ, Dept Chem, Beijing 100048, Peoples R China
[4] Univ N Carolina, Eshelman Sch Pharm, Chapel Hill, NC 27599 USA
[5] Drexel Univ, Dept Chem, Philadelphia, PA 19104 USA
关键词
amplification-by-polymerization; biosensors; genomic DNA detection; RAFT; ATRP; TRANSFER RADICAL POLYMERIZATION; SIGNAL AMPLIFICATION; SEX DETERMINATION; ELECTRON-TRANSFER; CHROMOSOME; MUTATION; GENE;
D O I
10.1021/acssensors.9b00133
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A polymerization reaction was employed as a signal amplification method to realize direct visualization of gender-specific DNA extracted from human blood in a polymerase chain reaction (PCR)-free fashion. Clear-distinction between X and Y chromosomes was observed by naked eyes for detector-free sensing purposes. The grown polymer films atop X and Y chromosomes were quantitatively measured by ellipsometry for thickness readings. Detection assays have been optimized for genomic DNA recognition to a maximum extent by varying the selection of the proper blocking reagents, the annealing temperature, and the annealing time. Traditional PCR and gel electrophoresis for amplicon identification were conducted in parallel for performance comparison. In the blind test for blood samples examined by the new approach, 25 out of 26 were correct and one was false negative, which was comparable to, if not better than, the PCR results. This is the first time our amplification-by polymerization technique is being used for chromosome DNA analysis. The potential of adopting the described sensing technique without PCR was demonstrated, which could further promote the development of a portable, PCR-free DNA sensing device for point-of-need applications.
引用
收藏
页码:992 / 1000
页数:17
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