| Literature DB >> 22243128 |
Hua Deng1, Yi Xu, Yanhua Liu, Zhijun Che, Huilin Guo, Shuxian Shan, Yun Sun, Xiaofang Liu, Keyang Huang, Xiaowei Ma, Yan Wu, Xing-Jie Liang.
Abstract
We developed a novel strategy for rapid colorimetric analysis of a specific DNA sequence by combining gold nanoparticles (AuNPs) with an asymmetric polymerase chain reaction (As-PCR). In the presence of the correct DNA template, the bound oligonucleotides on the surface of AuNPs selectively hybridized to form complementary sequences of single-stranded DNA (ssDNA) target generated from As-PCR. DNA hybridization resulted in self-assembly and aggregation of AuNPs, and a concomitant color change from ruby red to blue-purple occurred. This approach is simpler than previous methods, as it requires a simple mixture of the asymmetric PCR product with gold colloid conjugates. Thus, it is a convenient colorimetric method for specific nucleic acid sequence analysis with high specificity and sensitivity. Most importantly, the marked color change occurs at a picogram detection level after standing for several minutes at room temperature. Linear amplification minimizes the potential risk of PCR product cross-contamination. The efficiency to detect Bacillus anthracis in clinical samples clearly indicates the practical applicability of this approach.Entities:
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Year: 2012 PMID: 22243128 DOI: 10.1021/ac201713t
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986