NanoHDA: A nanoparticle-assisted isothermal amplification technique for genotyping assays

被引:0
作者
Abootaleb Sedighi
Christopher Oberc
Vicki Whitehall
Paul C. H. Li
机构
[1] Simon Fraser University,Department of Chemistry
[2] QIMR Berghofer Medical Research Institute,Department of Chemical and Physical Sciences
[3] University of Toronto,undefined
来源
Nano Research | 2017年 / 10卷
关键词
gold nanoparticle; isothermal DNA amplification; helicase; genotyping assay; colorectal cancer; single nucleotide polymorphism;
D O I
暂无
中图分类号
学科分类号
摘要
Isothermal methods, such as helicase-dependent amplification (HDA), have an advantage over polymerase chain reaction for DNA amplification owing to their ease of operation. Here, we developed a new HDA method that is nanoparticle-assisted, termed nanoHDA. This method uses gold nanoparticles (AuNPs) to improve the sensitivity and specificity of the isothermal method. In HDA, the denaturation of DNA templates is mediated by helicases, but this method is limited by the low denaturation efficiency of helicases. In this report, AuNPs with preferential affinity for single-stranded DNA (ssDNA) were utilized to improve the denaturation efficiency of helicases. The same affinity property of nanoparticles can also enhance specificity by suppressing primer-dimer formation. This nanoHDA method was employed to genotype the KRAS gene in genomic DNA samples from colorectal cancer patients, as achieved by the hybridization of nanoHDA amplicons using the NanoBioArray chip.
引用
收藏
页码:12 / 21
页数:9
相关论文
共 202 条
[1]  
Saiki R. K.(1985)Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia Science 230 1350-1354
[2]  
Scharf S.(2000)Loop-mediated isothermal amplification of DNA Nucleic Acids Res. 28 e63-232
[3]  
Faloona F.(1998)Mutation detection and singlemolecule counting using isothermal rolling-circle amplification Nat. Genet. 19 225-286
[4]  
Mullis K. B.(1991)NASBATM isothermal enzymatic in vitro nucleic acid amplification optimized for the diagnosis of HIV-1 infection J. Virol. Methods 35 273-1696
[5]  
Horn G. T.(1992)Strand displacement amplification—An isothermal, in vitro DNA amplification technique Nucleic Acids Res. 20 1691-800
[6]  
Erlich H. A.(2004)Helicase-dependent isothermal DNA amplification EMBO Rep. 5 795-2687
[7]  
Arnheim N.(2012)Automated detection of toxigenic Clostridium difficile in clinical samples: Isothermal tcdB amplification coupled to array-based detection J. Clin. Microbiol. 50 2681-248
[8]  
Notomi T.(2009)Helicase dependent OnChip-amplification and its use in multiplex pathogen detection Clin. Chim. Acta 403 244-458
[9]  
Okayama H.(2008)Application of isothermal helicase-dependent amplification with a disposable detection device in a simple sensitive stool test for toxigenic Clostridium difficile J. Mol. Diagn. 10 452-124
[10]  
Masubuchi H.(2008)Colorimetric detection of Helicobacter pylori DNA using isothermal helicase-dependent amplification and gold nanoparticle probes Diagn. Microbiol. Infect. Dis. 62 119-1536