Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules & College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, PR China.
Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules & College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, PR China.
Biosens Bioelectron. 2019 Oct 1;142:111532. doi: 10.1016/j.bios.2019.111532. Epub 2019 Jul 25.
In this paper, a novel label-free electrochemical impedance aptasensor for highly sensitive detection of IFN-γ based on target-induced exonuclease inhibition was constructed. For this purpose, we designed a DNA hairpin modified on the gold electrode whose loop was the aptamer of the IFN-γ, and the stem was 5'-thiol-modified. In the absence of IFN-γ, Exonuclease III (Exo III) and Exonuclease I (Exo I) digested the double-stranded and single-stranded strands of the hairpin DNA, respectively, causing smaller impedance value on the surface of the electrode. In the presence of IFN-γ, the function of Exo III was greatly inhibited by the binding of the aptamer with the target, and it stopped after cutting three bases of the hairpin DNA. Forming a major target-bound aptamer digestion product, it could not be digested by Exo I, so there was larger impedance on the electrode surface. The calibration curve for IFN-γ was linear in the range of 1 pM-50 nM with the detection limit (LOD) of 0.7 pM The proposed aptasensor proved good selectivity and reproducibility, and low cost. In addition, the biosensor was able to detect IFN-γ in serum samples successfully, which is expected to provide an efficient method for TB diagnosis at early stages.
本文构建了一种基于靶标诱导外切酶抑制的新型无标记电化学免疫传感器,用于高灵敏度检测 IFN-γ。为此,我们设计了一种修饰在金电极上的 DNA 发夹,其环为 IFN-γ 的适体,茎为 5'-硫醇修饰。在没有 IFN-γ 的情况下,核酸外切酶 III(Exo III)和核酸外切酶 I(Exo I)分别消化发夹 DNA 的双链和单链,导致电极表面的阻抗值较小。在存在 IFN-γ 的情况下,适体与靶标结合大大抑制了 Exo III 的功能,并且在切割发夹 DNA 的三个碱基后停止。形成主要的靶标结合适体消化产物,不能被 Exo I 消化,因此电极表面的阻抗较大。IFN-γ 的校准曲线在 1 pM-50 nM 范围内呈线性,检测限(LOD)为 0.7 pM。所提出的适体传感器表现出良好的选择性、重现性和低成本。此外,该生物传感器能够成功检测血清样本中的 IFN-γ,有望为早期结核病诊断提供一种有效的方法。