4.7 Article

Simple and accurate visual detection of single nucleotide polymorphism based on colloidal gold nucleic acid strip biosensor and primer-specific PCR

Journal

ANALYTICA CHIMICA ACTA
Volume 1093, Issue -, Pages 106-114

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2019.09.048

Keywords

Primer-specific PCR; Colloidal gold nucleic acid strip biosensor; Single nucleotide polymorphism; Cancer

Funding

  1. National Key Research and Development Program of China [2017YFA0700402]
  2. National Natural Science Foundation of China [21575058, 81771878, 81971658]
  3. Fundamental Research Funds for the Central Universities [Hust: 2016YXMS253, 2017KFXKJC002, 2018KFYXKJC048]

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Single nucleotide polymorphism (SNP) was associated with many human diseases, therefore, SNP detection was important for early diagnosis and clinical prognosis. Herein, a simple and accurate method for visual detection SNP sites (A/A, G/G, A/G) in CYP1A1 gene related to cancers based on colloidal gold nucleic acid strip biosensor and primer-specific polymerase chain reaction (PCR) was established. This method could directly distinguish SNP sites on strip biosensor by introducing twice PCR amplifications. The second PCR (primer-specific PCR) was performed using specific product of the first PCR as template, thus this twice PCR could reduce non-specific amplification greatly and obtain target product. In addition, single-strand or double-strand DNA (ssDNA or dsDNA) was accurately produced by introducing mismatched base at the 3' end of forward primers in primer-specific PCR. The designed strip biosensor could only combine with the ssDNA, thus visual detection of SNP could be achieved within 10 min by color difference of a pair of strips. 61 human blood samples by this method were identical with those of pyrosequencing. This method had the advantages of rapid, visual and low-cost and was expected to be applied in medical diagnosis. (C) 2019 Elsevier B.V. All rights reserved.

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