University of Maryland, College Park, MD 20742, United States.
Biosens Bioelectron. 2012 Feb 15;32(1):69-75. doi: 10.1016/j.bios.2011.11.040. Epub 2011 Dec 2.
An electronic platform to detect very small amounts of genomic DNA from bacteria without the need for PCR amplification and molecular labeling is described. The system uses carbon nanotube field-effect transistor (FET) arrays whose electrical properties are affected by minute electrical charges localized on their active regions. Two pathogenic strains of E. coli are used to evaluate the detection properties of the transistor arrays. Described herein are the results for detection of synthetic oligomers, unpurified and highly purified genomic DNA at various concentrations and their comparison against non-specific binding. In particular, the capture of genomic DNA of E. coli O157:H7 by a specific oligonucleotide probe coated onto the transistor array results in a significant shift in the threshold (gate-source) voltage (V(th)). By contrast the signal under the same procedure using a different strain, E. coli O45 that is non-complementary to the probe remained nearly constant. This work highlights the detection sensitivity and efficacy of this biosensor without stringent requirement for DNA sample preparation.
本文介绍了一种无需 PCR 扩增和分子标记即可检测细菌中极少量基因组 DNA 的电子平台。该系统使用碳纳米管场效应晶体管 (FET) 阵列,其电学性质受到其活性区域上局部微小电荷的影响。使用两种致病性大肠杆菌菌株来评估晶体管阵列的检测性能。本文描述了在不同浓度下检测合成寡核苷酸、未纯化和高度纯化的基因组 DNA 的结果,并将其与非特异性结合进行了比较。特别是,通过在晶体管阵列上涂覆特定的寡核苷酸探针来捕获大肠杆菌 O157:H7 的基因组 DNA,导致阈值 (栅源) 电压 (V(th)) 发生显著变化。相比之下,在使用不同菌株(与探针不互补的大肠杆菌 O45)进行相同程序时,信号几乎保持不变。这项工作突出了该生物传感器的检测灵敏度和效果,而无需对 DNA 样本进行严格的制备。