4.8 Article

Visual Detection of Single-Nucleotide Polymorphism with Hairpin Oligonucleotide-Functionalized Gold Nanoparticles

期刊

ANALYTICAL CHEMISTRY
卷 82, 期 17, 页码 7169-7177

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ac101275s

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资金

  1. North Dakota Experimental Program to Stimulate Competitive Research (EPS-CoR)
  2. North Dakota State University
  3. Guangdong Provincial Natural Science Foundation of China [06021655, 07001961, 07300648]
  4. Guangzhou Health Department, China [2006-ZDi-07]
  5. Guangdong Province Health Department Research Fund of China [A2007543]

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We report a simple, fast, and sensitive approach for visual detection of single-nucleotide polymorphism (SNP) based on hairpin oligonucleotide-functionalized gold nanopartide (HO-Au-NP) and lateral flow strip biosensor (LFSB). The results presented here expand on prior work (Mao, X.; Xu, H.; Zeng, Q.; Zeng, L.; Liu, G. Chem. Commun. 2009, 3065-3067.) by providing new approach to prepare HO-Au-NP conjugates with a deoxyadenosine triphosphate (dATP) blocker, which shortens the preparation time of the conjugates from 50 to 8 h and lowers the detection limit 500 times. A hairpin oligonucleotide modified with a thiol at the 5'-end and a biotin at the 3'-end was conjugated with Au-NP through a self-assembling process. Following a blocking step with dATP, the hairpin structure of HO and dATP embed the biotin groups, and make the biotin groups in close proximity to the Au-NP surface, leading to the biotins being inactive. The strategy of detecting SNP depends on the unique molecular recognition properties of HO to the perfect-matched DNA and single-base-mismatched DNA to generate different quantities of active biotin groups on the Au-NP surface. After hybridization reactions, the Au-NPs associated with the activated biotins are captured on the test zone of LFSB via the specific reaction between the activated biotin and preimmobilized streptavidin. Accumulation of Au-NPs produces the characteristic red bands, enabling visual detection of SNP. The preparations of HO-Au-NP conjugates with dATP and the parameters of assay were optimized systematically, and the abilities of detecting SNP were examined in details. The current approach is capable of discriminating as low as 10 pM of perfect-matched DNA and single-base-mismatched DNA within 25 min without instrumentation. Moreover, the approach provides a lower background and higher selectivity compared to the current molecular beacon-based SNP detection. The protocol should facilitate the simple, fast, and cost-effective screening of important SNPs and could readily find wide applications in molecular diagnosis laboratories and in point-of-care testing (field testing).

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