Institute of Bioengineering and Nanotechnology, 31 Biopolis Way, Singapore 138669.
Anal Chem. 2010 Jul 15;82(14):5958-64. doi: 10.1021/ac1003135.
A simple and sensitive electrical sensor array for polymerase chain reaction-free (PCR-free) messenger RNA (mRNA) expression profiling is described in this work. The sensor array, consisting of vertically aligned gold microband electrode/SiO(2)/gold microband electrode sandwich structures (nanogap sensors) in orthogonal configurations, was fabricated on a 1 cm x 1 cm silicon chip. A target mRNA was first hybridized with its specific capture probes (CP) on the bottom side of the nanogap, followed by a second hybridization (annealing) of its poly(A) tail with poly(T) annealing probes (AP) on the top side of the nanogap, holding the hybridized mRNA strands vertically across the nanogap. A subsequent metallization of the hybridized mRNA strands bridged the nanogap and consequently produced a substantial change in conductance, allowing ultrasensitive detection of mRNA without any amplification. Noticeable conductance changes were observed in the presence of as little as 0.10 fM mRNA. A linear relationship between the conductance and mRNA concentration was obtained from 0.50 fM to 1.0 pM with exceptional signal intensity. As little as a 50% difference in mRNA expression was successfully detected. The sensor array also exhibited excellent mismatch discrimination due to its unique vertically aligned nanostructure and the two-step hybridization.
本工作介绍了一种用于无聚合酶链反应(PCR-free)信使 RNA(mRNA)表达谱分析的简单、灵敏的电传感器阵列。该传感器阵列由垂直排列的金微带电极/SiO2/金微带电极三明治结构(纳米间隙传感器)以正交配置构成,在 1cm×1cm 的硅片上制造。目标 mRNA 首先与其特异性捕获探针(CP)在纳米间隙的底部杂交,然后其 poly(A)尾与纳米间隙顶部的 poly(T)退火探针(AP)进行第二次杂交(退火),使杂交的 mRNA 链垂直横跨纳米间隙。随后,杂交的 mRNA 链的金属化桥接了纳米间隙,从而导致电导发生实质性变化,无需任何扩增即可实现对 mRNA 的超灵敏检测。在存在低至 0.10fM 的 mRNA 时,就观察到了明显的电导变化。从 0.50fM 到 1.0pM ,可以获得与电导和 mRNA 浓度之间的线性关系,信号强度异常。成功检测到 mRNA 表达的低至 50%的差异。由于其独特的垂直排列纳米结构和两步杂交,该传感器阵列还表现出出色的错配辨别能力。