Wang Jun, Li Jinhua, Baca Alfred J, Hu Jingbo, Zhou Feimeng, Yan Wei, Pang Dai-Wen
Anal Chem. 2003 Aug 1;75(15):3941-5. doi: 10.1021/ac0344079.
Gold nanoparticle/streptavidin conjugates covered with 6-ferrocenylhexanethiol were attached onto a biotinylated DNA detection probe of a sandwich DNA complex. Due to the elasticity of the DNA strands, the ferrocene caps on gold nanoparticle/streptavidin conjugates are positioned in close proximity to the underlying electrode modified with a mixed DNA capture probe/hexanethiol self-assembled monolayer and can undergo reversible electron-transfer reactions. A detection level, down to 2.0 pM (10 amol for the 5 microL of sample needed) for oligodeoxynucleotide samples was obtained. The amplification of the voltammetric signals was attributed to the attachment of a large number of redox (ferrocene) markers per DNA duplex formed. The ferrocene oxidation current increased with the target concentration and began to level off at a target concentration of 10 nM. An Excellent linearity was found within the range between 6.9 and 150.0 pM and reasonable relative standard deviations (between 3.0 and 13.0%) were obtained. The amenability of this method to the analyses of polynucleotides (i.e., PCR products of the pre-S gene of hepatitis B virus in serum samples) was also demonstrated. The method is shown to be simple, selective, reproducible, and cost-effective and does not require labeling of the DNA targets.
覆盖有6-二茂铁基己硫醇的金纳米颗粒/链霉亲和素缀合物被连接到夹心DNA复合物的生物素化DNA检测探针上。由于DNA链的弹性,金纳米颗粒/链霉亲和素缀合物上的二茂铁帽靠近用混合DNA捕获探针/己硫醇自组装单层修饰的底层电极定位,并可进行可逆的电子转移反应。对于寡脱氧核苷酸样品,检测限低至2.0 pM(对于所需的5 μL样品为10 amol)。伏安信号的放大归因于每个形成的DNA双链体附着大量的氧化还原(二茂铁)标记物。二茂铁氧化电流随目标浓度增加,并在目标浓度为10 nM时开始趋于平稳。在6.9至150.0 pM范围内发现了良好的线性关系,并获得了合理的相对标准偏差(3.0%至13.0%)。该方法对多核苷酸(即血清样品中乙型肝炎病毒前S基因的PCR产物)分析的适用性也得到了证明。该方法显示出简单、选择性好、可重复且具有成本效益,并且不需要对DNA靶标进行标记。