Département de Chimie Moléculaire, UMR 5250, ICMG FR 2607, CNRS, Université Joseph Fourier Grenoble I, BP 53, 38041 Grenoble cedex 9, France.
Anal Chem. 2010 Feb 1;82(3):1066-72. doi: 10.1021/ac9024329.
An ultrahigh performance impedimetric DNA sensor is presented showing detection limits in the femtomolar range. This electrochemical setup was constructed initially by electrogeneration of poly(11-pyrrol-1-yl-undecanoic acid N(alpha'),N(alpha)-bis(carboxymethyl)-L-lysine amide) (poly(pyrrole-NTA)) film. The latter was then modified by the coordination of Cu(2+) ions onto the chelating NTA centers followed by the immobilization of the ssHIV-DNA previously modified by a polyhistidine tag by affinity binding. The immobilization of the DNA probe and hybridization with the complementary target ssHIV-DNA were investigated using fluorescence microscopy and quantified with quartz crystal microbalance experiments leading to DNA probe and duplex coverage of 1.7 x 10(-11) and 7.7 x 10(-12) mol cm(-2), respectively. The duplex formation was corroborated by amperometric measurements through the duplex labeling by a glucose oxidase. In the presence of hydroquinone as redox indicator, the DNA sensor was applied to the impedimetric detection of target DNA without a labeling step. A linear quantification of the HIV DNA target was carried out in the range 10(-15) to 10(-8) mol L(-1).
一种超高性能的阻抗 DNA 传感器,其检测限可达飞摩尔级。该电化学装置最初通过聚(11-吡咯-1-基-十一烷酸 N(alpha'),N(alpha)-双(羧甲基)-L-赖氨酸酰胺)(聚(吡咯-NTA))薄膜的电生成来构建。然后,通过将 Cu(2+) 离子配位到螯合 NTA 中心,随后通过亲和结合固定先前通过多组氨酸标记修饰的 ssHIV-DNA,对其进行修饰。使用荧光显微镜研究 DNA 探针的固定和与互补靶 ssHIV-DNA 的杂交,并通过石英晶体微天平实验进行定量,导致 DNA 探针和双链体的覆盖率分别为 1.7 x 10(-11) 和 7.7 x 10(-12) mol cm(-2)。通过葡萄糖氧化酶对双链体进行标记,通过安培测量证实了双链体的形成。在氢醌作为氧化还原指示剂的存在下,该 DNA 传感器无需标记步骤即可应用于目标 DNA 的阻抗检测。在 10(-15) 到 10(-8) mol L(-1) 的范围内,对 HIV DNA 靶标进行了线性定量。