4.7 Article

Simultaneous detection of four specific DNAs fragments based on two-dimensional bimetallic MOF nanosheets

Journal

MICROCHEMICAL JOURNAL
Volume 182, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.microc.2022.107918

Keywords

Metallic organic framework nanosheet; Fluorescent probes; HAV; HBV; HCV; HIV

Funding

  1. National Natural Science Foundation of China (NSFC) [21465010]
  2. Enshi Technology Plan Project [XYJ2020000002]
  3. Open Foundation of Key Laboratory of Biologic Resources Protection and Utilization of Hubei Province [PT012207, PT012213]
  4. Special Funds for Double First-Class Construction in Hubei Province

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We have developed a quantitative analysis method based on two-dimensional bimetallic MOF nanosheets for simultaneous detection of four specific DNA fragments. This method utilizes fluorescent probes and a quencher to achieve rapid detection of T-DNAs, and exhibits low detection limits, good selectivity, and high sensitivity.
We have developed quantitative analysis method for simultaneous detection of four specific DNAs fragments based on two-dimensional bimetallic MOF nanosheets Co/Fe(1:1) MOF. In this analytical method, four different dyes were labeled on the complementary sequences of four different target DNAs (T-DNAs) as fluorescent probes, and Co/Fe(1:1) MOF was chosen as quencher. In the absence of T-DNAs, four fluorescent probes were adsorbed on the Co/Fe(1:1) MOF by pi-pi stacking, and the dyes were close to Co/Fe(1:1) MOF, their fluorescence is quenched by Co/Fe(1:1) MOF through photoinduced electron transfer. In the presence of T-DNAs, four different T-DNAs react with the corresponding fluorescent probe to form double strands DNA, which cannot be adsorbed by Co/Fe(1:1) MOF, and the fluorescence of dyes was recovered. Under the optimal conditions, the fluorescence intensities of four dyes all exhibited good linear dependence on corresponding concentration of T-DNAs. The detection limits of HAV, HBV, HCV and HIV were 0.032 nmol/L, 0.037 nmol/L, 0.53 nmol/L and 0.18 nmol/L (3 sigma, n = 9), respectively. The analytical method has low detection limit, good selectivity and high sensitivity, and can be used to detect T-DNAs in vitro.

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